Canonical Allele Identifier: CA421212602

Gene: SPTA1

Linked Data

• MyVariant Identifiers: chr1:g.158582670T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612880T>A , CM000663.2:g.158612880T>A	GRCh38
NC_000001.10:g.158582670T>A , CM000663.1:g.158582670T>A	GRCh37
NC_000001.9:g.156849294T>A	NCBI36
NG_011474.1:g.78837A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7071A>T MANE Select	ENSP00000495214.1:p.Ile2357=
ENST00000368147.8:c.7071A>T	ENSP00000357129.4:p.Ile2357=
ENST00000481212.5:n.512A>T
ENST00000498708.1:n.503A>T
ENST00000614909.4:c.7071A>T	ENSP00000482595.1:p.Ile2357=
NM_003126.2:c.7071A>T	NP_003117.2:p.Ile2357=
XM_011509916.1:c.7071A>T	XP_011508218.1:p.Ile2357=
XM_011509917.1:c.7053A>T	XP_011508219.1:p.Ile2351=
NM_003126.3:c.7071A>T	NP_003117.2:p.Ile2357=
XM_011509916.2:c.7071A>T	XP_011508218.1:p.Ile2357=
XM_011509917.3:c.7053A>T	XP_011508219.1:p.Ile2351=
NM_003126.4:c.7071A>T MANE Select	NP_003117.2:p.Ile2357=