Linked Data
dbSNP Id:
rs62063857
ExAC:
17:44076665 A / G
gnomAD v2:
17-44076665-A-G
gnomAD v3:
17-45999299-A-G
gnomAD v4:
17-45999299-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.45999299A>G , CM000679.2:g.45999299A>G | GRCh38 |
| NC_000017.10:g.44076665A>G , CM000679.1:g.44076665A>G | GRCh37 |
| NC_000017.9:g.41432502A>G | NCBI36 |
| NG_007398.1:g.109879A>G | |
| NG_007398.2:g.109837A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000420682.7:c.735+2635A>G (MAPT) | ENSP00000413056.2:n.735+2635A>G | |
| ENST00000703922.1:c.735+2635A>G (MAPT) | ENSP00000515557.1:n.735+2635A>G | |
| ENST00000703923.1:c.648+2635A>G (MAPT) | ENSP00000515558.1:n.648+2635A>G | |
| ENST00000703924.1:c.735+2635A>G (MAPT) | ENSP00000515559.1:n.735+2635A>G | |
| ENST00000703978.1:c.822+2635A>G (MAPT) | ENSP00000515600.1:n.822+2635A>G | |
| ENST00000703979.1:n.686+2635A>G (MAPT) | ||
| ENST00000703980.1:n.54+2635A>G (MAPT) | ||
| ENST00000262410.10:c.1998+2635A>G (MAPT) MANE Select | ENSP00000262410.6:n.1998+2635A>G | |
| ENST00000344290.10:c.1800+2635A>G (MAPT) | ENSP00000340820.6:n.1800+2635A>G | |
| ENST00000351559.10:c.822+2635A>G (MAPT) | ENSP00000303214.7:n.822+2635A>G | |
| ENST00000535772.6:c.735+2635A>G (MAPT) | ENSP00000443028.2:n.735+2635A>G | |
| ENST00000680542.1:c.735+2635A>G (MAPT) | ENSP00000505258.1:n.735+2635A>G | |
| ENST00000680674.1:c.648+2635A>G (MAPT) | ENSP00000505478.1:n.648+2635A>G | |
| ENST00000262410.9:c.1773+2635A>G (MAPT) | ENSP00000262410.5:n.1773+2635A>G | |
| ENST00000334239.12:c.648+2635A>G (MAPT) | ENSP00000334886.8:n.648+2635A>G | |
| ENST00000340799.9:c.735+2635A>G (MAPT) | ENSP00000340438.5:n.735+2635A>G | |
| ENST00000344290.9:c.1827+2635A>G (MAPT) | ENSP00000340820.5:n.1827+2635A>G | |
| ENST00000351559.9:c.822+2635A>G (MAPT) | ENSP00000303214.7:n.822+2635A>G | |
| ENST00000415613.6:c.1827+2635A>G (MAPT) | ENSP00000410838.2:n.1827+2635A>G | |
| ENST00000420682.6:c.735+2635A>G (MAPT) | ENSP00000413056.2:n.735+2635A>G | |
| ENST00000431008.7:c.822+2635A>G (MAPT) | ENSP00000389250.3:n.822+2635A>G | |
| ENST00000446361.7:c.648+2635A>G (MAPT) | ENSP00000408975.3:n.648+2635A>G | |
| ENST00000535772.5:c.822+2635A>G (MAPT) | ENSP00000443028.1:n.822+2635A>G | |
| ENST00000537309.1:c.20A>G (STH) MANE Select | ENSP00000443168.1:p.Gln7Arg | |
| ENST00000570299.5:n.776+2635A>G (MAPT) | ||
| ENST00000571987.5:c.1773+2635A>G (MAPT) | ENSP00000458742.1:n.1773+2635A>G | |
| ENST00000574436.5:c.822+2635A>G (MAPT) | ENSP00000460965.1:n.822+2635A>G | |
| ENST00000576518.1:n.6107+2635A>G (MAPT) | ||
| NM_001007532.2:c.20A>G (STH) | NP_001007533.1:p.Gln7Arg | |
| NM_001123066.3:c.1827+2635A>G (MAPT) | NP_001116538.2:n.1827+2635A>G | |
| NM_001123067.3:c.735+2635A>G (MAPT) | NP_001116539.1:n.735+2635A>G | |
| NM_001203251.1:c.735+2635A>G (MAPT) | NP_001190180.1:n.735+2635A>G | |
| NM_001203252.1:c.822+2635A>G (MAPT) | NP_001190181.1:n.822+2635A>G | |
| NM_005910.5:c.822+2635A>G (MAPT) | NP_005901.2:n.822+2635A>G | |
| NM_016834.4:c.648+2635A>G (MAPT) | NP_058518.1:n.648+2635A>G | |
| NM_016835.4:c.1773+2635A>G (MAPT) | NP_058519.3:n.1773+2635A>G | |
| NM_016841.4:c.648+2635A>G (MAPT) | NP_058525.1:n.648+2635A>G | |
| XM_005257362.3:c.2085+2635A>G (MAPT) | XP_005257419.1:n.2085+2635A>G | |
| XM_005257364.3:c.1998+2635A>G (MAPT) | XP_005257421.1:n.1998+2635A>G | |
| XM_005257365.3:c.2085+2635A>G (MAPT) | XP_005257422.1:n.2085+2635A>G | |
| XM_005257366.2:c.1911+2635A>G (MAPT) | XP_005257423.1:n.1911+2635A>G | |
| XM_005257367.3:c.1887+2635A>G (MAPT) | XP_005257424.1:n.1887+2635A>G | |
| XM_005257368.3:c.1887+2635A>G (MAPT) | XP_005257425.1:n.1887+2635A>G | |
| XM_005257369.3:c.1020+2635A>G (MAPT) | XP_005257426.1:n.1020+2635A>G | |
| XM_005257370.3:c.933+2635A>G (MAPT) | XP_005257427.1:n.933+2635A>G | |
| XM_005257371.3:c.846+2635A>G (MAPT) | XP_005257428.1:n.846+2635A>G | |
| XM_005257362.4:c.2085+2635A>G (MAPT) | XP_005257419.1:n.2085+2635A>G | |
| XM_005257364.4:c.1998+2635A>G (MAPT) | XP_005257421.1:n.1998+2635A>G | |
| XM_005257365.4:c.2085+2635A>G (MAPT) | XP_005257422.1:n.2085+2635A>G | |
| XM_005257366.3:c.1911+2635A>G (MAPT) | XP_005257423.1:n.1911+2635A>G | |
| XM_005257367.4:c.1887+2635A>G (MAPT) | XP_005257424.1:n.1887+2635A>G | |
| XM_005257368.4:c.1887+2635A>G (MAPT) | XP_005257425.1:n.1887+2635A>G | |
| XM_005257369.4:c.1020+2635A>G (MAPT) | XP_005257426.1:n.1020+2635A>G | |
| XM_005257370.4:c.933+2635A>G (MAPT) | XP_005257427.1:n.933+2635A>G | |
| XM_005257371.4:c.846+2635A>G (MAPT) | XP_005257428.1:n.846+2635A>G | |
| NM_001007532.3:c.20A>G (STH) MANE Select | NP_001007533.1:p.Gln7Arg | |
| NM_001203251.2:c.735+2635A>G (MAPT) | NP_001190180.1:n.735+2635A>G | |
| NM_001377265.1:c.1998+2635A>G (MAPT) MANE Select | NP_001364194.1:n.1998+2635A>G | |
| NM_001377266.1:c.1800+2635A>G (MAPT) | NP_001364195.1:n.1800+2635A>G | |
| NM_001377267.1:c.735+2635A>G (MAPT) | NP_001364196.1:n.735+2635A>G | |
| NM_001377268.1:c.648+2635A>G (MAPT) | NP_001364197.1:n.648+2635A>G | |
| NM_016834.5:c.648+2635A>G (MAPT) | NP_058518.1:n.648+2635A>G | |
| NM_016841.5:c.648+2635A>G (MAPT) | NP_058525.1:n.648+2635A>G | |
| NR_165166.1:n.746+2635A>G (MAPT) | ||
| NM_001123066.4:c.1827+2635A>G (MAPT) | NP_001116538.2:n.1827+2635A>G | |
| NM_001123067.4:c.735+2635A>G (MAPT) | NP_001116539.1:n.735+2635A>G | |
| NM_001203252.2:c.822+2635A>G (MAPT) | NP_001190181.1:n.822+2635A>G | |
| NM_005910.6:c.822+2635A>G (MAPT) | NP_005901.2:n.822+2635A>G | |
| NM_016835.5:c.1773+2635A>G (MAPT) | NP_058519.3:n.1773+2635A>G |