Canonical Allele Identifier: CA399984539

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44101455G>A (hg19) ; chr17:g.46024089G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46024089G>A , CM000679.2:g.46024089G>A	GRCh38
NC_000017.10:g.44101455G>A , CM000679.1:g.44101455G>A	GRCh37
NC_000017.9:g.41457300G>A	NCBI36
NG_007398.1:g.134677G>A
NG_007398.2:g.134627G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.1157G>A	ENSP00000413056.2:p.Gly386Asp
ENST00000703922.1:c.1157G>A	ENSP00000515557.1:p.Gly386Asp
ENST00000703923.1:c.1070G>A	ENSP00000515558.1:p.Gly357Asp
ENST00000703924.1:c.1157G>A	ENSP00000515559.1:p.Gly386Asp
ENST00000703978.1:c.1244G>A	ENSP00000515600.1:p.Gly415Asp
ENST00000703980.1:n.470G>A
ENST00000703981.1:n.428G>A
ENST00000703982.1:n.662G>A
ENST00000262410.10:c.2420G>A MANE Select	ENSP00000262410.6:p.Gly807Asp
ENST00000344290.10:c.2129G>A	ENSP00000340820.6:p.Gly710Asp
ENST00000351559.10:c.1244G>A	ENSP00000303214.7:p.Gly415Asp
ENST00000535772.6:c.1064G>A	ENSP00000443028.2:p.Gly355Asp
ENST00000680542.1:c.1157G>A	ENSP00000505258.1:p.Gly386Asp
ENST00000680674.1:c.1193G>A	ENSP00000505478.1:p.Gly398Asp
ENST00000262410.9:c.2195G>A	ENSP00000262410.5:p.Gly732Asp
ENST00000334239.12:c.977G>A	ENSP00000334886.8:p.Gly326Asp
ENST00000340799.9:c.1157G>A	ENSP00000340438.5:p.Gly386Asp
ENST00000344290.9:c.2249G>A	ENSP00000340820.5:p.Gly750Asp
ENST00000351559.9:c.1244G>A	ENSP00000303214.7:p.Gly415Asp
ENST00000415613.6:c.2249G>A	ENSP00000410838.2:p.Gly750Asp
ENST00000420682.6:c.1157G>A	ENSP00000413056.2:p.Gly386Asp
ENST00000431008.7:c.1151G>A	ENSP00000389250.3:p.Gly384Asp
ENST00000446361.7:c.1070G>A	ENSP00000408975.3:p.Gly357Asp
ENST00000535772.5:c.1151G>A	ENSP00000443028.1:p.Gly384Asp
ENST00000571987.5:c.2195G>A	ENSP00000458742.1:p.Gly732Asp
ENST00000574436.5:c.1244G>A	ENSP00000460965.1:p.Gly415Asp
ENST00000576518.1:n.6436G>A
NM_001123066.3:c.2249G>A	NP_001116538.2:p.Gly750Asp
NM_001123067.3:c.1157G>A	NP_001116539.1:p.Gly386Asp
NM_001203251.1:c.1064G>A	NP_001190180.1:p.Gly355Asp
NM_001203252.1:c.1151G>A	NP_001190181.1:p.Gly384Asp
NM_005910.5:c.1244G>A	NP_005901.2:p.Gly415Asp
NM_016834.4:c.1070G>A	NP_058518.1:p.Gly357Asp
NM_016835.4:c.2195G>A	NP_058519.3:p.Gly732Asp
NM_016841.4:c.977G>A	NP_058525.1:p.Gly326Asp
XM_005257362.3:c.2507G>A	XP_005257419.1:p.Gly836Asp
XM_005257364.3:c.2420G>A	XP_005257421.1:p.Gly807Asp
XM_005257365.3:c.2414G>A	XP_005257422.1:p.Gly805Asp
XM_005257366.2:c.2333G>A	XP_005257423.1:p.Gly778Asp
XM_005257367.3:c.2309G>A	XP_005257424.1:p.Gly770Asp
XM_005257368.3:c.2216G>A	XP_005257425.1:p.Gly739Asp
XM_005257369.3:c.1442G>A	XP_005257426.1:p.Gly481Asp
XM_005257370.3:c.1355G>A	XP_005257427.1:p.Gly452Asp
XM_005257371.3:c.1268G>A	XP_005257428.1:p.Gly423Asp
XM_005257362.4:c.2507G>A	XP_005257419.1:p.Gly836Asp
XM_005257364.4:c.2420G>A	XP_005257421.1:p.Gly807Asp
XM_005257365.4:c.2414G>A	XP_005257422.1:p.Gly805Asp
XM_005257366.3:c.2333G>A	XP_005257423.1:p.Gly778Asp
XM_005257367.4:c.2309G>A	XP_005257424.1:p.Gly770Asp
XM_005257368.4:c.2216G>A	XP_005257425.1:p.Gly739Asp
XM_005257369.4:c.1442G>A	XP_005257426.1:p.Gly481Asp
XM_005257370.4:c.1355G>A	XP_005257427.1:p.Gly452Asp
XM_005257371.4:c.1268G>A	XP_005257428.1:p.Gly423Asp
NM_001203251.2:c.1064G>A	NP_001190180.1:p.Gly355Asp
NM_001377265.1:c.2420G>A MANE Select	NP_001364194.1:p.Gly807Asp
NM_001377266.1:c.2129G>A	NP_001364195.1:p.Gly710Asp
NM_001377267.1:c.772-1028G>A	NP_001364196.1:n.772-1028G>A
NM_001377268.1:c.977G>A	NP_001364197.1:p.Gly326Asp
NM_016834.5:c.1070G>A	NP_058518.1:p.Gly357Asp
NM_016841.5:c.977G>A	NP_058525.1:p.Gly326Asp
NR_165166.1:n.1075G>A
NM_001123066.4:c.2249G>A	NP_001116538.2:p.Gly750Asp
NM_001123067.4:c.1157G>A	NP_001116539.1:p.Gly386Asp
NM_001203252.2:c.1151G>A	NP_001190181.1:p.Gly384Asp
NM_005910.6:c.1244G>A	NP_005901.2:p.Gly415Asp
NM_016835.5:c.2195G>A	NP_058519.3:p.Gly732Asp