Canonical Allele Identifier: CA399984268

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44101327A>C (hg19) ; chr17:g.46023961A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46023961A>C , CM000679.2:g.46023961A>C	GRCh38
NC_000017.10:g.44101327A>C , CM000679.1:g.44101327A>C	GRCh37
NC_000017.9:g.41457172A>C	NCBI36
NG_007398.1:g.134549A>C
NG_007398.2:g.134499A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000420682.7:c.1029A>C	ENSP00000413056.2:p.Glu343Asp
ENST00000703922.1:c.1029A>C	ENSP00000515557.1:p.Glu343Asp
ENST00000703923.1:c.942A>C	ENSP00000515558.1:p.Glu314Asp
ENST00000703924.1:c.1029A>C	ENSP00000515559.1:p.Glu343Asp
ENST00000703978.1:c.1116A>C	ENSP00000515600.1:p.Glu372Asp
ENST00000703980.1:n.342A>C
ENST00000703981.1:n.300A>C
ENST00000703982.1:n.534A>C
ENST00000262410.10:c.2292A>C MANE Select	ENSP00000262410.6:p.Glu764Asp
ENST00000344290.10:c.2001A>C	ENSP00000340820.6:p.Glu667Asp
ENST00000351559.10:c.1116A>C	ENSP00000303214.7:p.Glu372Asp
ENST00000535772.6:c.936A>C	ENSP00000443028.2:p.Glu312Asp
ENST00000680542.1:c.1029A>C	ENSP00000505258.1:p.Glu343Asp
ENST00000680674.1:c.1065A>C	ENSP00000505478.1:p.Glu355Asp
ENST00000262410.9:c.2067A>C	ENSP00000262410.5:p.Glu689Asp
ENST00000334239.12:c.849A>C	ENSP00000334886.8:p.Glu283Asp
ENST00000340799.9:c.1029A>C	ENSP00000340438.5:p.Glu343Asp
ENST00000344290.9:c.2121A>C	ENSP00000340820.5:p.Glu707Asp
ENST00000351559.9:c.1116A>C	ENSP00000303214.7:p.Glu372Asp
ENST00000415613.6:c.2121A>C	ENSP00000410838.2:p.Glu707Asp
ENST00000420682.6:c.1029A>C	ENSP00000413056.2:p.Glu343Asp
ENST00000431008.7:c.1023A>C	ENSP00000389250.3:p.Glu341Asp
ENST00000446361.7:c.942A>C	ENSP00000408975.3:p.Glu314Asp
ENST00000535772.5:c.1023A>C	ENSP00000443028.1:p.Glu341Asp
ENST00000571987.5:c.2067A>C	ENSP00000458742.1:p.Glu689Asp
ENST00000574436.5:c.1116A>C	ENSP00000460965.1:p.Glu372Asp
ENST00000576518.1:n.6308A>C
NM_001123066.3:c.2121A>C	NP_001116538.2:p.Glu707Asp
NM_001123067.3:c.1029A>C	NP_001116539.1:p.Glu343Asp
NM_001203251.1:c.936A>C	NP_001190180.1:p.Glu312Asp
NM_001203252.1:c.1023A>C	NP_001190181.1:p.Glu341Asp
NM_005910.5:c.1116A>C	NP_005901.2:p.Glu372Asp
NM_016834.4:c.942A>C	NP_058518.1:p.Glu314Asp
NM_016835.4:c.2067A>C	NP_058519.3:p.Glu689Asp
NM_016841.4:c.849A>C	NP_058525.1:p.Glu283Asp
XM_005257362.3:c.2379A>C	XP_005257419.1:p.Glu793Asp
XM_005257364.3:c.2292A>C	XP_005257421.1:p.Glu764Asp
XM_005257365.3:c.2286A>C	XP_005257422.1:p.Glu762Asp
XM_005257366.2:c.2205A>C	XP_005257423.1:p.Glu735Asp
XM_005257367.3:c.2181A>C	XP_005257424.1:p.Glu727Asp
XM_005257368.3:c.2088A>C	XP_005257425.1:p.Glu696Asp
XM_005257369.3:c.1314A>C	XP_005257426.1:p.Glu438Asp
XM_005257370.3:c.1227A>C	XP_005257427.1:p.Glu409Asp
XM_005257371.3:c.1140A>C	XP_005257428.1:p.Glu380Asp
XM_005257362.4:c.2379A>C	XP_005257419.1:p.Glu793Asp
XM_005257364.4:c.2292A>C	XP_005257421.1:p.Glu764Asp
XM_005257365.4:c.2286A>C	XP_005257422.1:p.Glu762Asp
XM_005257366.3:c.2205A>C	XP_005257423.1:p.Glu735Asp
XM_005257367.4:c.2181A>C	XP_005257424.1:p.Glu727Asp
XM_005257368.4:c.2088A>C	XP_005257425.1:p.Glu696Asp
XM_005257369.4:c.1314A>C	XP_005257426.1:p.Glu438Asp
XM_005257370.4:c.1227A>C	XP_005257427.1:p.Glu409Asp
XM_005257371.4:c.1140A>C	XP_005257428.1:p.Glu380Asp
NM_001203251.2:c.936A>C	NP_001190180.1:p.Glu312Asp
NM_001377265.1:c.2292A>C MANE Select	NP_001364194.1:p.Glu764Asp
NM_001377266.1:c.2001A>C	NP_001364195.1:p.Glu667Asp
NM_001377267.1:c.772-1156A>C	NP_001364196.1:n.772-1156A>C
NM_001377268.1:c.849A>C	NP_001364197.1:p.Glu283Asp
NM_016834.5:c.942A>C	NP_058518.1:p.Glu314Asp
NM_016841.5:c.849A>C	NP_058525.1:p.Glu283Asp
NR_165166.1:n.947A>C
NM_001123066.4:c.2121A>C	NP_001116538.2:p.Glu707Asp
NM_001123067.4:c.1029A>C	NP_001116539.1:p.Glu343Asp
NM_001203252.2:c.1023A>C	NP_001190181.1:p.Glu341Asp
NM_005910.6:c.1116A>C	NP_005901.2:p.Glu372Asp
NM_016835.5:c.2067A>C	NP_058519.3:p.Glu689Asp