Canonical Allele Identifier: CA278887

Gene: SPTA1

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158661410C>T , CM000663.2:g.158661410C>T	GRCh38
NC_000001.10:g.158631200C>T , CM000663.1:g.158631200C>T	GRCh37
NC_000001.9:g.156897824C>T	NCBI36
NG_011474.1:g.30307G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.2465-1G>A MANE Select	ENSP00000495214.1:n.2465-1G>A
ENST00000647256.1:n.64G>A
ENST00000368147.8:c.2465-1G>A	ENSP00000357129.4:n.2465-1G>A
ENST00000614909.4:c.2465-1G>A	ENSP00000482595.1:n.2465-1G>A
NM_003126.2:c.2465-1G>A	NP_003117.2:n.2465-1G>A
XM_011509916.1:c.2465-1G>A	XP_011508218.1:n.2465-1G>A
XM_011509917.1:c.2465-1G>A	XP_011508219.1:n.2465-1G>A
XM_011509918.1:c.2465-1G>A	XP_011508220.1:n.2465-1G>A
XM_011509919.1:c.2465-1G>A	XP_011508221.1:n.2465-1G>A
XR_921911.1:n.2578-1G>A
XR_921912.1:n.2583-1G>A
NM_003126.3:c.2465-1G>A	NP_003117.2:n.2465-1G>A
XM_011509916.2:c.2465-1G>A	XP_011508218.1:n.2465-1G>A
XM_011509917.3:c.2465-1G>A	XP_011508219.1:n.2465-1G>A
XM_011509918.3:c.2465-1G>A	XP_011508220.1:n.2465-1G>A
XM_011509919.3:c.2465-1G>A	XP_011508221.1:n.2465-1G>A
XR_921911.3:n.2591-1G>A
XR_921912.2:n.2593-1G>A
NM_003126.4:c.2465-1G>A MANE Select	NP_003117.2:n.2465-1G>A