Canonical Allele Identifier: CA1139955631

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158615625C= , CM000663.2:g.158615625C=	GRCh38
NC_000001.10:g.158585415C= , CM000663.1:g.158585415C=	GRCh37
NC_000001.9:g.156852039C=	NCBI36
NG_011474.1:g.76092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.6601-222G= MANE Select	ENSP00000495214.1:n.6601-222G=
ENST00000368147.8:c.6601-222G=	ENSP00000357129.4:n.6601-222G=
ENST00000492934.1:n.116-222G=
ENST00000498708.1:n.33-222G=
ENST00000614909.4:c.6601-222G=	ENSP00000482595.1:n.6601-222G=
NM_003126.2:c.6601-222G=	NP_003117.2:n.6601-222G=
XM_011509916.1:c.6601-222G=	XP_011508218.1:n.6601-222G=
XM_011509917.1:c.6583-222G=	XP_011508219.1:n.6583-222G=
NM_003126.3:c.6601-222G=	NP_003117.2:n.6601-222G=
XM_011509916.2:c.6601-222G=	XP_011508218.1:n.6601-222G=
XM_011509917.3:c.6583-222G=	XP_011508219.1:n.6583-222G=
NM_003126.4:c.6601-222G= MANE Select	NP_003117.2:n.6601-222G=