Canonical Allele Identifier: CA889966020

Gene: SPTA1

Linked Data

• dbSNP Id: rs1156339826
• gnomAD v4: 1-158613082-C-T
• MyVariant Identifiers: chr1:g.158582872C>T (hg19) ; chr1:g.158613082C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158613082C>T , CM000663.2:g.158613082C>T	GRCh38
NC_000001.10:g.158582872C>T , CM000663.1:g.158582872C>T	GRCh37
NC_000001.9:g.156849496C>T	NCBI36
NG_011474.1:g.78635G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.6990-121G>A MANE Select	ENSP00000495214.1:n.6990-121G>A
ENST00000368147.8:c.6990-121G>A	ENSP00000357129.4:n.6990-121G>A
ENST00000481212.5:n.431-121G>A
ENST00000498708.1:n.422-121G>A
ENST00000614909.4:c.6990-121G>A	ENSP00000482595.1:n.6990-121G>A
NM_003126.2:c.6990-121G>A	NP_003117.2:n.6990-121G>A
XM_011509916.1:c.6990-121G>A	XP_011508218.1:n.6990-121G>A
XM_011509917.1:c.6972-121G>A	XP_011508219.1:n.6972-121G>A
NM_003126.3:c.6990-121G>A	NP_003117.2:n.6990-121G>A
XM_011509916.2:c.6990-121G>A	XP_011508218.1:n.6990-121G>A
XM_011509917.3:c.6972-121G>A	XP_011508219.1:n.6972-121G>A
NM_003126.4:c.6990-121G>A MANE Select	NP_003117.2:n.6990-121G>A