Canonical Allele Identifier: CA500371190

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44091659T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46014293T>C , CM000679.2:g.46014293T>C	GRCh38
NC_000017.10:g.44091659T>C , CM000679.1:g.44091659T>C	GRCh37
NC_000017.9:g.41447496T>C	NCBI36
NG_007398.1:g.124873T>C
NG_007398.2:g.124831T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.879T>C	ENSP00000413056.2:p.Cys293=
ENST00000703922.1:c.879T>C	ENSP00000515557.1:p.Cys293=
ENST00000703923.1:c.792T>C	ENSP00000515558.1:p.Cys264=
ENST00000703924.1:c.879T>C	ENSP00000515559.1:p.Cys293=
ENST00000703978.1:c.966T>C	ENSP00000515600.1:p.Cys322=
ENST00000703979.1:n.737T>C
ENST00000703980.1:n.192T>C
ENST00000703981.1:n.135T>C
ENST00000262410.10:c.2142T>C MANE Select	ENSP00000262410.6:p.Cys714=
ENST00000344290.10:c.1851T>C	ENSP00000340820.6:p.Cys617=
ENST00000351559.10:c.966T>C	ENSP00000303214.7:p.Cys322=
ENST00000535772.6:c.786T>C	ENSP00000443028.2:p.Cys262=
ENST00000680542.1:c.879T>C	ENSP00000505258.1:p.Cys293=
ENST00000680674.1:c.792T>C	ENSP00000505478.1:p.Cys264=
ENST00000262410.9:c.1917T>C	ENSP00000262410.5:p.Cys639=
ENST00000334239.12:c.699T>C	ENSP00000334886.8:p.Cys233=
ENST00000340799.9:c.879T>C	ENSP00000340438.5:p.Cys293=
ENST00000344290.9:c.1971T>C	ENSP00000340820.5:p.Cys657=
ENST00000351559.9:c.966T>C	ENSP00000303214.7:p.Cys322=
ENST00000415613.6:c.1971T>C	ENSP00000410838.2:p.Cys657=
ENST00000420682.6:c.879T>C	ENSP00000413056.2:p.Cys293=
ENST00000431008.7:c.873T>C	ENSP00000389250.3:p.Cys291=
ENST00000446361.7:c.792T>C	ENSP00000408975.3:p.Cys264=
ENST00000535772.5:c.873T>C	ENSP00000443028.1:p.Cys291=
ENST00000570299.5:n.777-4325T>C
ENST00000571987.5:c.1917T>C	ENSP00000458742.1:p.Cys639=
ENST00000574436.5:c.966T>C	ENSP00000460965.1:p.Cys322=
ENST00000576518.1:n.6158T>C
NM_001123066.3:c.1971T>C	NP_001116538.2:p.Cys657=
NM_001123067.3:c.879T>C	NP_001116539.1:p.Cys293=
NM_001203251.1:c.786T>C	NP_001190180.1:p.Cys262=
NM_001203252.1:c.873T>C	NP_001190181.1:p.Cys291=
NM_005910.5:c.966T>C	NP_005901.2:p.Cys322=
NM_016834.4:c.792T>C	NP_058518.1:p.Cys264=
NM_016835.4:c.1917T>C	NP_058519.3:p.Cys639=
NM_016841.4:c.699T>C	NP_058525.1:p.Cys233=
XM_005257362.3:c.2229T>C	XP_005257419.1:p.Cys743=
XM_005257364.3:c.2142T>C	XP_005257421.1:p.Cys714=
XM_005257365.3:c.2136T>C	XP_005257422.1:p.Cys712=
XM_005257366.2:c.2055T>C	XP_005257423.1:p.Cys685=
XM_005257367.3:c.2031T>C	XP_005257424.1:p.Cys677=
XM_005257368.3:c.1938T>C	XP_005257425.1:p.Cys646=
XM_005257369.3:c.1164T>C	XP_005257426.1:p.Cys388=
XM_005257370.3:c.1077T>C	XP_005257427.1:p.Cys359=
XM_005257371.3:c.990T>C	XP_005257428.1:p.Cys330=
XM_005257362.4:c.2229T>C	XP_005257419.1:p.Cys743=
XM_005257364.4:c.2142T>C	XP_005257421.1:p.Cys714=
XM_005257365.4:c.2136T>C	XP_005257422.1:p.Cys712=
XM_005257366.3:c.2055T>C	XP_005257423.1:p.Cys685=
XM_005257367.4:c.2031T>C	XP_005257424.1:p.Cys677=
XM_005257368.4:c.1938T>C	XP_005257425.1:p.Cys646=
XM_005257369.4:c.1164T>C	XP_005257426.1:p.Cys388=
XM_005257370.4:c.1077T>C	XP_005257427.1:p.Cys359=
XM_005257371.4:c.990T>C	XP_005257428.1:p.Cys330=
NM_001203251.2:c.786T>C	NP_001190180.1:p.Cys262=
NM_001377265.1:c.2142T>C MANE Select	NP_001364194.1:p.Cys714=
NM_001377266.1:c.1851T>C	NP_001364195.1:p.Cys617=
NM_001377267.1:c.771+15T>C	NP_001364196.1:n.771+15T>C
NM_001377268.1:c.699T>C	NP_001364197.1:p.Cys233=
NM_016834.5:c.792T>C	NP_058518.1:p.Cys264=
NM_016841.5:c.699T>C	NP_058525.1:p.Cys233=
NR_165166.1:n.797T>C
NM_001123066.4:c.1971T>C	NP_001116538.2:p.Cys657=
NM_001123067.4:c.879T>C	NP_001116539.1:p.Cys293=
NM_001203252.2:c.873T>C	NP_001190181.1:p.Cys291=
NM_005910.6:c.966T>C	NP_005901.2:p.Cys322=
NM_016835.5:c.1917T>C	NP_058519.3:p.Cys639=