Canonical Allele Identifier: CA399983747

Gene: MAPT

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46018675C>A , CM000679.2:g.46018675C>A	GRCh38
NC_000017.10:g.44096041C>A , CM000679.1:g.44096041C>A	GRCh37
NC_000017.9:g.41451888C>A	NCBI36
NG_007398.1:g.129265C>A
NG_007398.2:g.129213C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.968C>A	ENSP00000413056.2:p.Ser323Ter
ENST00000703922.1:c.968C>A	ENSP00000515557.1:p.Ser323Ter
ENST00000703923.1:c.881C>A	ENSP00000515558.1:p.Ser294Ter
ENST00000703924.1:c.968C>A	ENSP00000515559.1:p.Ser323Ter
ENST00000703978.1:c.1055C>A	ENSP00000515600.1:p.Ser352Ter
ENST00000703979.1:n.826C>A
ENST00000703980.1:n.281C>A
ENST00000703981.1:n.239C>A
ENST00000703982.1:n.473C>A
ENST00000262410.10:c.2231C>A MANE Select	ENSP00000262410.6:p.Ser744Ter
ENST00000344290.10:c.1940C>A	ENSP00000340820.6:p.Ser647Ter
ENST00000351559.10:c.1055C>A	ENSP00000303214.7:p.Ser352Ter
ENST00000535772.6:c.875C>A	ENSP00000443028.2:p.Ser292Ter
ENST00000680542.1:c.968C>A	ENSP00000505258.1:p.Ser323Ter
ENST00000680674.1:c.1004C>A	ENSP00000505478.1:p.Ser335Ter
ENST00000262410.9:c.2006C>A	ENSP00000262410.5:p.Ser669Ter
ENST00000334239.12:c.788C>A	ENSP00000334886.8:p.Ser263Ter
ENST00000340799.9:c.968C>A	ENSP00000340438.5:p.Ser323Ter
ENST00000344290.9:c.2060C>A	ENSP00000340820.5:p.Ser687Ter
ENST00000351559.9:c.1055C>A	ENSP00000303214.7:p.Ser352Ter
ENST00000415613.6:c.2060C>A	ENSP00000410838.2:p.Ser687Ter
ENST00000420682.6:c.968C>A	ENSP00000413056.2:p.Ser323Ter
ENST00000431008.7:c.962C>A	ENSP00000389250.3:p.Ser321Ter
ENST00000446361.7:c.881C>A	ENSP00000408975.3:p.Ser294Ter
ENST00000535772.5:c.962C>A	ENSP00000443028.1:p.Ser321Ter
ENST00000570299.5:n.834C>A
ENST00000571987.5:c.2006C>A	ENSP00000458742.1:p.Ser669Ter
ENST00000574436.5:c.1055C>A	ENSP00000460965.1:p.Ser352Ter
ENST00000576518.1:n.6247C>A
NM_001123066.3:c.2060C>A	NP_001116538.2:p.Ser687Ter
NM_001123067.3:c.968C>A	NP_001116539.1:p.Ser323Ter
NM_001203251.1:c.875C>A	NP_001190180.1:p.Ser292Ter
NM_001203252.1:c.962C>A	NP_001190181.1:p.Ser321Ter
NM_005910.5:c.1055C>A	NP_005901.2:p.Ser352Ter
NM_016834.4:c.881C>A	NP_058518.1:p.Ser294Ter
NM_016835.4:c.2006C>A	NP_058519.3:p.Ser669Ter
NM_016841.4:c.788C>A	NP_058525.1:p.Ser263Ter
XM_005257362.3:c.2318C>A	XP_005257419.1:p.Ser773Ter
XM_005257364.3:c.2231C>A	XP_005257421.1:p.Ser744Ter
XM_005257365.3:c.2225C>A	XP_005257422.1:p.Ser742Ter
XM_005257366.2:c.2144C>A	XP_005257423.1:p.Ser715Ter
XM_005257367.3:c.2120C>A	XP_005257424.1:p.Ser707Ter
XM_005257368.3:c.2027C>A	XP_005257425.1:p.Ser676Ter
XM_005257369.3:c.1253C>A	XP_005257426.1:p.Ser418Ter
XM_005257370.3:c.1166C>A	XP_005257427.1:p.Ser389Ter
XM_005257371.3:c.1079C>A	XP_005257428.1:p.Ser360Ter
XM_005257362.4:c.2318C>A	XP_005257419.1:p.Ser773Ter
XM_005257364.4:c.2231C>A	XP_005257421.1:p.Ser744Ter
XM_005257365.4:c.2225C>A	XP_005257422.1:p.Ser742Ter
XM_005257366.3:c.2144C>A	XP_005257423.1:p.Ser715Ter
XM_005257367.4:c.2120C>A	XP_005257424.1:p.Ser707Ter
XM_005257368.4:c.2027C>A	XP_005257425.1:p.Ser676Ter
XM_005257369.4:c.1253C>A	XP_005257426.1:p.Ser418Ter
XM_005257370.4:c.1166C>A	XP_005257427.1:p.Ser389Ter
XM_005257371.4:c.1079C>A	XP_005257428.1:p.Ser360Ter
NM_001203251.2:c.875C>A	NP_001190180.1:p.Ser292Ter
NM_001377265.1:c.2231C>A MANE Select	NP_001364194.1:p.Ser744Ter
NM_001377266.1:c.1940C>A	NP_001364195.1:p.Ser647Ter
NM_001377267.1:c.771+4397C>A	NP_001364196.1:n.771+4397C>A
NM_001377268.1:c.788C>A	NP_001364197.1:p.Ser263Ter
NM_016834.5:c.881C>A	NP_058518.1:p.Ser294Ter
NM_016841.5:c.788C>A	NP_058525.1:p.Ser263Ter
NR_165166.1:n.886C>A
NM_001123066.4:c.2060C>A	NP_001116538.2:p.Ser687Ter
NM_001123067.4:c.968C>A	NP_001116539.1:p.Ser323Ter
NM_001203252.2:c.962C>A	NP_001190181.1:p.Ser321Ter
NM_005910.6:c.1055C>A	NP_005901.2:p.Ser352Ter
NM_016835.5:c.2006C>A	NP_058519.3:p.Ser669Ter