Canonical Allele Identifier: CA500644004

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44073916G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45996550G>T , CM000679.2:g.45996550G>T	GRCh38
NC_000017.10:g.44073916G>T , CM000679.1:g.44073916G>T	GRCh37
NC_000017.9:g.41429753G>T	NCBI36
NG_007398.1:g.107130G>T
NG_007398.2:g.107088G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.621G>T	ENSP00000413056.2:p.Pro207=
ENST00000703922.1:c.621G>T	ENSP00000515557.1:p.Pro207=
ENST00000703923.1:c.534G>T	ENSP00000515558.1:p.Pro178=
ENST00000703924.1:c.621G>T	ENSP00000515559.1:p.Pro207=
ENST00000703978.1:c.708G>T	ENSP00000515600.1:p.Pro236=
ENST00000703979.1:n.572G>T
ENST00000262410.10:c.1884G>T MANE Select	ENSP00000262410.6:p.Pro628=
ENST00000344290.10:c.1686G>T	ENSP00000340820.6:p.Pro562=
ENST00000351559.10:c.708G>T	ENSP00000303214.7:p.Pro236=
ENST00000535772.6:c.621G>T	ENSP00000443028.2:p.Pro207=
ENST00000680542.1:c.621G>T	ENSP00000505258.1:p.Pro207=
ENST00000680674.1:c.534G>T	ENSP00000505478.1:p.Pro178=
ENST00000262410.9:c.1659G>T	ENSP00000262410.5:p.Pro553=
ENST00000334239.12:c.534G>T	ENSP00000334886.8:p.Pro178=
ENST00000340799.9:c.621G>T	ENSP00000340438.5:p.Pro207=
ENST00000344290.9:c.1713G>T	ENSP00000340820.5:p.Pro571=
ENST00000351559.9:c.708G>T	ENSP00000303214.7:p.Pro236=
ENST00000415613.6:c.1713G>T	ENSP00000410838.2:p.Pro571=
ENST00000420682.6:c.621G>T	ENSP00000413056.2:p.Pro207=
ENST00000431008.7:c.708G>T	ENSP00000389250.3:p.Pro236=
ENST00000446361.7:c.534G>T	ENSP00000408975.3:p.Pro178=
ENST00000535772.5:c.708G>T	ENSP00000443028.1:p.Pro236=
ENST00000570299.5:n.662G>T
ENST00000571987.5:c.1659G>T	ENSP00000458742.1:p.Pro553=
ENST00000574436.5:c.708G>T	ENSP00000460965.1:p.Pro236=
ENST00000576518.1:n.5993G>T
NM_001123066.3:c.1713G>T	NP_001116538.2:p.Pro571=
NM_001123067.3:c.621G>T	NP_001116539.1:p.Pro207=
NM_001203251.1:c.621G>T	NP_001190180.1:p.Pro207=
NM_001203252.1:c.708G>T	NP_001190181.1:p.Pro236=
NM_005910.5:c.708G>T	NP_005901.2:p.Pro236=
NM_016834.4:c.534G>T	NP_058518.1:p.Pro178=
NM_016835.4:c.1659G>T	NP_058519.3:p.Pro553=
NM_016841.4:c.534G>T	NP_058525.1:p.Pro178=
XM_005257362.3:c.1971G>T	XP_005257419.1:p.Pro657=
XM_005257364.3:c.1884G>T	XP_005257421.1:p.Pro628=
XM_005257365.3:c.1971G>T	XP_005257422.1:p.Pro657=
XM_005257366.2:c.1797G>T	XP_005257423.1:p.Pro599=
XM_005257367.3:c.1773G>T	XP_005257424.1:p.Pro591=
XM_005257368.3:c.1773G>T	XP_005257425.1:p.Pro591=
XM_005257369.3:c.906G>T	XP_005257426.1:p.Pro302=
XM_005257370.3:c.819G>T	XP_005257427.1:p.Pro273=
XM_005257371.3:c.732G>T	XP_005257428.1:p.Pro244=
XM_005257362.4:c.1971G>T	XP_005257419.1:p.Pro657=
XM_005257364.4:c.1884G>T	XP_005257421.1:p.Pro628=
XM_005257365.4:c.1971G>T	XP_005257422.1:p.Pro657=
XM_005257366.3:c.1797G>T	XP_005257423.1:p.Pro599=
XM_005257367.4:c.1773G>T	XP_005257424.1:p.Pro591=
XM_005257368.4:c.1773G>T	XP_005257425.1:p.Pro591=
XM_005257369.4:c.906G>T	XP_005257426.1:p.Pro302=
XM_005257370.4:c.819G>T	XP_005257427.1:p.Pro273=
XM_005257371.4:c.732G>T	XP_005257428.1:p.Pro244=
NM_001203251.2:c.621G>T	NP_001190180.1:p.Pro207=
NM_001377265.1:c.1884G>T MANE Select	NP_001364194.1:p.Pro628=
NM_001377266.1:c.1686G>T	NP_001364195.1:p.Pro562=
NM_001377267.1:c.621G>T	NP_001364196.1:p.Pro207=
NM_001377268.1:c.534G>T	NP_001364197.1:p.Pro178=
NM_016834.5:c.534G>T	NP_058518.1:p.Pro178=
NM_016841.5:c.534G>T	NP_058525.1:p.Pro178=
NR_165166.1:n.632G>T
NM_001123066.4:c.1713G>T	NP_001116538.2:p.Pro571=
NM_001123067.4:c.621G>T	NP_001116539.1:p.Pro207=
NM_001203252.2:c.708G>T	NP_001190181.1:p.Pro236=
NM_005910.6:c.708G>T	NP_005901.2:p.Pro236=
NM_016835.5:c.1659G>T	NP_058519.3:p.Pro553=