Canonical Allele Identifier: CA2648555630

Gene: SPTA1

Linked Data

• gnomAD v4: 1-158612786-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.158612786A>C , CM000663.2:g.158612786A>C	GRCh38
NC_000001.10:g.158582576A>C , CM000663.1:g.158582576A>C	GRCh37
NC_000001.9:g.156849200A>C	NCBI36
NG_011474.1:g.78931T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643759.2:c.7134+31T>G MANE Select	ENSP00000495214.1:n.7134+31T>G
ENST00000368147.8:c.7134+31T>G	ENSP00000357129.4:n.7134+31T>G
ENST00000481212.5:n.606T>G
ENST00000498708.1:n.597T>G
ENST00000614909.4:c.7134+31T>G	ENSP00000482595.1:n.7134+31T>G
NM_003126.2:c.7134+31T>G	NP_003117.2:n.7134+31T>G
XM_011509916.1:c.7134+31T>G	XP_011508218.1:n.7134+31T>G
XM_011509917.1:c.7116+31T>G	XP_011508219.1:n.7116+31T>G
NM_003126.3:c.7134+31T>G	NP_003117.2:n.7134+31T>G
XM_011509916.2:c.7134+31T>G	XP_011508218.1:n.7134+31T>G
XM_011509917.3:c.7116+31T>G	XP_011508219.1:n.7116+31T>G
NM_003126.4:c.7134+31T>G MANE Select	NP_003117.2:n.7134+31T>G