Canonical Allele Identifier: CA1143800087

Gene: SPTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612835G= , CM000663.2:g.158612835G=	GRCh38
NC_000001.10:g.158582625G= , CM000663.1:g.158582625G=	GRCh37
NC_000001.9:g.156849249G=	NCBI36
NG_011474.1:g.78882C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7116C= MANE Select	ENSP00000495214.1:p.Thr2372=
ENST00000368147.8:c.7116C=	ENSP00000357129.4:p.Thr2372=
ENST00000481212.5:n.557C=
ENST00000498708.1:n.548C=
ENST00000614909.4:c.7116C=	ENSP00000482595.1:p.Thr2372=
NM_003126.2:c.7116C=	NP_003117.2:p.Thr2372=
XM_011509916.1:c.7116C=	XP_011508218.1:p.Thr2372=
XM_011509917.1:c.7098C=	XP_011508219.1:p.Thr2366=
NM_003126.3:c.7116C=	NP_003117.2:p.Thr2372=
XM_011509916.2:c.7116C=	XP_011508218.1:p.Thr2372=
XM_011509917.3:c.7098C=	XP_011508219.1:p.Thr2366=
NM_003126.4:c.7116C= MANE Select	NP_003117.2:p.Thr2372=