Canonical Allele Identifier: CA1182317

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158635957C>T , CM000663.2:g.158635957C>T	GRCh38
NC_000001.10:g.158605747C>T , CM000663.1:g.158605747C>T	GRCh37
NC_000001.9:g.156872371C>T	NCBI36
NG_011474.1:g.55760G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.5388G>A MANE Select	ENSP00000495214.1:p.Gln1796=
ENST00000368147.8:c.5388G>A	ENSP00000357129.4:p.Gln1796=
ENST00000614909.4:c.5388G>A	ENSP00000482595.1:p.Gln1796=
NM_003126.2:c.5388G>A	NP_003117.2:p.Gln1796=
XM_011509916.1:c.5388G>A	XP_011508218.1:p.Gln1796=
XM_011509917.1:c.5388G>A	XP_011508219.1:p.Gln1796=
XM_011509918.1:c.5388G>A	XP_011508220.1:p.Gln1796=
XM_011509919.1:c.*91G>A	XP_011508221.1:n.*91G>A
XR_921911.1:n.5501G>A
NM_003126.3:c.5388G>A	NP_003117.2:p.Gln1796=
XM_011509916.2:c.5388G>A	XP_011508218.1:p.Gln1796=
XM_011509917.3:c.5388G>A	XP_011508219.1:p.Gln1796=
XM_011509918.3:c.5388G>A	XP_011508220.1:p.Gln1796=
XM_011509919.3:c.*91G>A	XP_011508221.1:n.*91G>A
XR_921911.3:n.5514G>A
NM_003126.4:c.5388G>A MANE Select	NP_003117.2:p.Gln1796=