Canonical Allele Identifier: CA399984533
Gene: MAPT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46024085A>T , CM000679.2:g.46024085A>T GRCh38
NC_000017.10:g.44101451A>T , CM000679.1:g.44101451A>T GRCh37
NC_000017.9:g.41457296A>T NCBI36
NG_007398.1:g.134673A>T
NG_007398.2:g.134623A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.1153A>T ENSP00000413056.2:p.Thr385Ser
ENST00000703922.1:c.1153A>T ENSP00000515557.1:p.Thr385Ser
ENST00000703923.1:c.1066A>T ENSP00000515558.1:p.Thr356Ser
ENST00000703924.1:c.1153A>T ENSP00000515559.1:p.Thr385Ser
ENST00000703978.1:c.1240A>T ENSP00000515600.1:p.Thr414Ser
ENST00000703980.1:n.466A>T
ENST00000703981.1:n.424A>T
ENST00000703982.1:n.658A>T
ENST00000262410.10:c.2416A>T MANE Select ENSP00000262410.6:p.Thr806Ser
ENST00000344290.10:c.2125A>T ENSP00000340820.6:p.Thr709Ser
ENST00000351559.10:c.1240A>T ENSP00000303214.7:p.Thr414Ser
ENST00000535772.6:c.1060A>T ENSP00000443028.2:p.Thr354Ser
ENST00000680542.1:c.1153A>T ENSP00000505258.1:p.Thr385Ser
ENST00000680674.1:c.1189A>T ENSP00000505478.1:p.Thr397Ser
ENST00000262410.9:c.2191A>T ENSP00000262410.5:p.Thr731Ser
ENST00000334239.12:c.973A>T ENSP00000334886.8:p.Thr325Ser
ENST00000340799.9:c.1153A>T ENSP00000340438.5:p.Thr385Ser
ENST00000344290.9:c.2245A>T ENSP00000340820.5:p.Thr749Ser
ENST00000351559.9:c.1240A>T ENSP00000303214.7:p.Thr414Ser
ENST00000415613.6:c.2245A>T ENSP00000410838.2:p.Thr749Ser
ENST00000420682.6:c.1153A>T ENSP00000413056.2:p.Thr385Ser
ENST00000431008.7:c.1147A>T ENSP00000389250.3:p.Thr383Ser
ENST00000446361.7:c.1066A>T ENSP00000408975.3:p.Thr356Ser
ENST00000535772.5:c.1147A>T ENSP00000443028.1:p.Thr383Ser
ENST00000571987.5:c.2191A>T ENSP00000458742.1:p.Thr731Ser
ENST00000574436.5:c.1240A>T ENSP00000460965.1:p.Thr414Ser
ENST00000576518.1:n.6432A>T
NM_001123066.3:c.2245A>T NP_001116538.2:p.Thr749Ser
NM_001123067.3:c.1153A>T NP_001116539.1:p.Thr385Ser
NM_001203251.1:c.1060A>T NP_001190180.1:p.Thr354Ser
NM_001203252.1:c.1147A>T NP_001190181.1:p.Thr383Ser
NM_005910.5:c.1240A>T NP_005901.2:p.Thr414Ser
NM_016834.4:c.1066A>T NP_058518.1:p.Thr356Ser
NM_016835.4:c.2191A>T NP_058519.3:p.Thr731Ser
NM_016841.4:c.973A>T NP_058525.1:p.Thr325Ser
XM_005257362.3:c.2503A>T XP_005257419.1:p.Thr835Ser
XM_005257364.3:c.2416A>T XP_005257421.1:p.Thr806Ser
XM_005257365.3:c.2410A>T XP_005257422.1:p.Thr804Ser
XM_005257366.2:c.2329A>T XP_005257423.1:p.Thr777Ser
XM_005257367.3:c.2305A>T XP_005257424.1:p.Thr769Ser
XM_005257368.3:c.2212A>T XP_005257425.1:p.Thr738Ser
XM_005257369.3:c.1438A>T XP_005257426.1:p.Thr480Ser
XM_005257370.3:c.1351A>T XP_005257427.1:p.Thr451Ser
XM_005257371.3:c.1264A>T XP_005257428.1:p.Thr422Ser
XM_005257362.4:c.2503A>T XP_005257419.1:p.Thr835Ser
XM_005257364.4:c.2416A>T XP_005257421.1:p.Thr806Ser
XM_005257365.4:c.2410A>T XP_005257422.1:p.Thr804Ser
XM_005257366.3:c.2329A>T XP_005257423.1:p.Thr777Ser
XM_005257367.4:c.2305A>T XP_005257424.1:p.Thr769Ser
XM_005257368.4:c.2212A>T XP_005257425.1:p.Thr738Ser
XM_005257369.4:c.1438A>T XP_005257426.1:p.Thr480Ser
XM_005257370.4:c.1351A>T XP_005257427.1:p.Thr451Ser
XM_005257371.4:c.1264A>T XP_005257428.1:p.Thr422Ser
NM_001203251.2:c.1060A>T NP_001190180.1:p.Thr354Ser
NM_001377265.1:c.2416A>T MANE Select NP_001364194.1:p.Thr806Ser
NM_001377266.1:c.2125A>T NP_001364195.1:p.Thr709Ser
NM_001377267.1:c.772-1032A>T NP_001364196.1:n.772-1032A>T
NM_001377268.1:c.973A>T NP_001364197.1:p.Thr325Ser
NM_016834.5:c.1066A>T NP_058518.1:p.Thr356Ser
NM_016841.5:c.973A>T NP_058525.1:p.Thr325Ser
NR_165166.1:n.1071A>T
NM_001123066.4:c.2245A>T NP_001116538.2:p.Thr749Ser
NM_001123067.4:c.1153A>T NP_001116539.1:p.Thr385Ser
NM_001203252.2:c.1147A>T NP_001190181.1:p.Thr383Ser
NM_005910.6:c.1240A>T NP_005901.2:p.Thr414Ser
NM_016835.5:c.2191A>T NP_058519.3:p.Thr731Ser