Canonical Allele Identifier: CA1183652

Gene: SPTA1

Linked Data

• ClinVar Variation Id: 293033
• ClinVar RCV Id: RCV000285045 ; RCV000338799 ; RCV000374835 ; RCV000963778
• dbSNP Id: rs73020251
• ExAC: 1:158639351 C / G
• gnomAD v2: 1-158639351-C-G
• gnomAD v3: 1-158669561-C-G
• gnomAD v4: 1-158669561-C-G
• MyVariant Identifiers: chr1:g.158639351C>G (hg19) ; chr1:g.158669561C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158669561C>G , CM000663.2:g.158669561C>G	GRCh38
NC_000001.10:g.158639351C>G , CM000663.1:g.158639351C>G	GRCh37
NC_000001.9:g.156905975C>G	NCBI36
NG_011474.1:g.22156G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.1680G>C MANE Select	ENSP00000495214.1:p.Leu560=
ENST00000368147.8:c.1680G>C	ENSP00000357129.4:p.Leu560=
ENST00000614909.4:c.1680G>C	ENSP00000482595.1:p.Leu560=
NM_003126.2:c.1680G>C	NP_003117.2:p.Leu560=
XM_011509916.1:c.1680G>C	XP_011508218.1:p.Leu560=
XM_011509917.1:c.1680G>C	XP_011508219.1:p.Leu560=
XM_011509918.1:c.1680G>C	XP_011508220.1:p.Leu560=
XM_011509919.1:c.1680G>C	XP_011508221.1:p.Leu560=
XR_921911.1:n.1793G>C
XR_921912.1:n.1798G>C
NM_003126.3:c.1680G>C	NP_003117.2:p.Leu560=
XM_011509916.2:c.1680G>C	XP_011508218.1:p.Leu560=
XM_011509917.3:c.1680G>C	XP_011508219.1:p.Leu560=
XM_011509918.3:c.1680G>C	XP_011508220.1:p.Leu560=
XM_011509919.3:c.1680G>C	XP_011508221.1:p.Leu560=
XR_921911.3:n.1806G>C
XR_921912.2:n.1808G>C
NM_003126.4:c.1680G>C MANE Select	NP_003117.2:p.Leu560=