Canonical Allele Identifier: CA1201536900
Gene: SPTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158612795G= , CM000663.2:g.158612795G= GRCh38
NC_000001.10:g.158582585G= , CM000663.1:g.158582585G= GRCh37
NC_000001.9:g.156849209G= NCBI36
NG_011474.1:g.78922C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000643759.2:c.7134+22C= MANE Select ENSP00000495214.1:n.7134+22C=
ENST00000368147.8:c.7134+22C= ENSP00000357129.4:n.7134+22C=
ENST00000481212.5:n.597C=
ENST00000498708.1:n.588C=
ENST00000614909.4:c.7134+22C= ENSP00000482595.1:n.7134+22C=
NM_003126.2:c.7134+22C= NP_003117.2:n.7134+22C=
XM_011509916.1:c.7134+22C= XP_011508218.1:n.7134+22C=
XM_011509917.1:c.7116+22C= XP_011508219.1:n.7116+22C=
NM_003126.3:c.7134+22C= NP_003117.2:n.7134+22C=
XM_011509916.2:c.7134+22C= XP_011508218.1:n.7134+22C=
XM_011509917.3:c.7116+22C= XP_011508219.1:n.7116+22C=
NM_003126.4:c.7134+22C= MANE Select NP_003117.2:n.7134+22C=