Canonical Allele Identifier: CA343025384

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158654926T>A (hg19) ; chr1:g.158685136T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158685136T>A , CM000663.2:g.158685136T>A	GRCh38
NC_000001.10:g.158654926T>A , CM000663.1:g.158654926T>A	GRCh37
NC_000001.9:g.156921550T>A	NCBI36
NG_011474.1:g.6581A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000643759.2:c.236A>T MANE Select	ENSP00000495214.1:p.Lys79Met
ENST00000368147.8:c.236A>T	ENSP00000357129.4:p.Lys79Met
ENST00000467387.1:c.132+104A>T	ENSP00000476485.1:n.132+104A>T
ENST00000614909.4:c.236A>T	ENSP00000482595.1:p.Lys79Met
NM_003126.2:c.236A>T	NP_003117.2:p.Lys79Met
XM_011509916.1:c.236A>T	XP_011508218.1:p.Lys79Met
XM_011509917.1:c.236A>T	XP_011508219.1:p.Lys79Met
XM_011509918.1:c.236A>T	XP_011508220.1:p.Lys79Met
XM_011509919.1:c.236A>T	XP_011508221.1:p.Lys79Met
XR_921911.1:n.349A>T
XR_921912.1:n.354A>T
NM_003126.3:c.236A>T	NP_003117.2:p.Lys79Met
XM_011509916.2:c.236A>T	XP_011508218.1:p.Lys79Met
XM_011509917.3:c.236A>T	XP_011508219.1:p.Lys79Met
XM_011509918.3:c.236A>T	XP_011508220.1:p.Lys79Met
XM_011509919.3:c.236A>T	XP_011508221.1:p.Lys79Met
XR_921911.3:n.362A>T
XR_921912.2:n.364A>T
NM_003126.4:c.236A>T MANE Select	NP_003117.2:p.Lys79Met