Canonical Allele Identifier: CA500371251

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44096033A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46018667A>G , CM000679.2:g.46018667A>G	GRCh38
NC_000017.10:g.44096033A>G , CM000679.1:g.44096033A>G	GRCh37
NC_000017.9:g.41451880A>G	NCBI36
NG_007398.1:g.129257A>G
NG_007398.2:g.129205A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.960A>G	ENSP00000413056.2:p.Arg320=
ENST00000703922.1:c.960A>G	ENSP00000515557.1:p.Arg320=
ENST00000703923.1:c.873A>G	ENSP00000515558.1:p.Arg291=
ENST00000703924.1:c.960A>G	ENSP00000515559.1:p.Arg320=
ENST00000703978.1:c.1047A>G	ENSP00000515600.1:p.Arg349=
ENST00000703979.1:n.818A>G
ENST00000703980.1:n.273A>G
ENST00000703981.1:n.231A>G
ENST00000703982.1:n.465A>G
ENST00000262410.10:c.2223A>G MANE Select	ENSP00000262410.6:p.Arg741=
ENST00000344290.10:c.1932A>G	ENSP00000340820.6:p.Arg644=
ENST00000351559.10:c.1047A>G	ENSP00000303214.7:p.Arg349=
ENST00000535772.6:c.867A>G	ENSP00000443028.2:p.Arg289=
ENST00000680542.1:c.960A>G	ENSP00000505258.1:p.Arg320=
ENST00000680674.1:c.996A>G	ENSP00000505478.1:p.Arg332=
ENST00000262410.9:c.1998A>G	ENSP00000262410.5:p.Arg666=
ENST00000334239.12:c.780A>G	ENSP00000334886.8:p.Arg260=
ENST00000340799.9:c.960A>G	ENSP00000340438.5:p.Arg320=
ENST00000344290.9:c.2052A>G	ENSP00000340820.5:p.Arg684=
ENST00000351559.9:c.1047A>G	ENSP00000303214.7:p.Arg349=
ENST00000415613.6:c.2052A>G	ENSP00000410838.2:p.Arg684=
ENST00000420682.6:c.960A>G	ENSP00000413056.2:p.Arg320=
ENST00000431008.7:c.954A>G	ENSP00000389250.3:p.Arg318=
ENST00000446361.7:c.873A>G	ENSP00000408975.3:p.Arg291=
ENST00000535772.5:c.954A>G	ENSP00000443028.1:p.Arg318=
ENST00000570299.5:n.826A>G
ENST00000571987.5:c.1998A>G	ENSP00000458742.1:p.Arg666=
ENST00000574436.5:c.1047A>G	ENSP00000460965.1:p.Arg349=
ENST00000576518.1:n.6239A>G
NM_001123066.3:c.2052A>G	NP_001116538.2:p.Arg684=
NM_001123067.3:c.960A>G	NP_001116539.1:p.Arg320=
NM_001203251.1:c.867A>G	NP_001190180.1:p.Arg289=
NM_001203252.1:c.954A>G	NP_001190181.1:p.Arg318=
NM_005910.5:c.1047A>G	NP_005901.2:p.Arg349=
NM_016834.4:c.873A>G	NP_058518.1:p.Arg291=
NM_016835.4:c.1998A>G	NP_058519.3:p.Arg666=
NM_016841.4:c.780A>G	NP_058525.1:p.Arg260=
XM_005257362.3:c.2310A>G	XP_005257419.1:p.Arg770=
XM_005257364.3:c.2223A>G	XP_005257421.1:p.Arg741=
XM_005257365.3:c.2217A>G	XP_005257422.1:p.Arg739=
XM_005257366.2:c.2136A>G	XP_005257423.1:p.Arg712=
XM_005257367.3:c.2112A>G	XP_005257424.1:p.Arg704=
XM_005257368.3:c.2019A>G	XP_005257425.1:p.Arg673=
XM_005257369.3:c.1245A>G	XP_005257426.1:p.Arg415=
XM_005257370.3:c.1158A>G	XP_005257427.1:p.Arg386=
XM_005257371.3:c.1071A>G	XP_005257428.1:p.Arg357=
XM_005257362.4:c.2310A>G	XP_005257419.1:p.Arg770=
XM_005257364.4:c.2223A>G	XP_005257421.1:p.Arg741=
XM_005257365.4:c.2217A>G	XP_005257422.1:p.Arg739=
XM_005257366.3:c.2136A>G	XP_005257423.1:p.Arg712=
XM_005257367.4:c.2112A>G	XP_005257424.1:p.Arg704=
XM_005257368.4:c.2019A>G	XP_005257425.1:p.Arg673=
XM_005257369.4:c.1245A>G	XP_005257426.1:p.Arg415=
XM_005257370.4:c.1158A>G	XP_005257427.1:p.Arg386=
XM_005257371.4:c.1071A>G	XP_005257428.1:p.Arg357=
NM_001203251.2:c.867A>G	NP_001190180.1:p.Arg289=
NM_001377265.1:c.2223A>G MANE Select	NP_001364194.1:p.Arg741=
NM_001377266.1:c.1932A>G	NP_001364195.1:p.Arg644=
NM_001377267.1:c.771+4389A>G	NP_001364196.1:n.771+4389A>G
NM_001377268.1:c.780A>G	NP_001364197.1:p.Arg260=
NM_016834.5:c.873A>G	NP_058518.1:p.Arg291=
NM_016841.5:c.780A>G	NP_058525.1:p.Arg260=
NR_165166.1:n.878A>G
NM_001123066.4:c.2052A>G	NP_001116538.2:p.Arg684=
NM_001123067.4:c.960A>G	NP_001116539.1:p.Arg320=
NM_001203252.2:c.954A>G	NP_001190181.1:p.Arg318=
NM_005910.6:c.1047A>G	NP_005901.2:p.Arg349=
NM_016835.5:c.1998A>G	NP_058519.3:p.Arg666=