Canonical Allele Identifier: CA1184197
Community Standard Title: NM_003126.4(SPTA1):c.326C>T (p.Ser109Phe)
Gene: SPTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158683435G>A , CM000663.2:g.158683435G>A GRCh38
NC_000001.10:g.158653225G>A , CM000663.1:g.158653225G>A GRCh37
NC_000001.9:g.156919849G>A NCBI36
NG_011474.1:g.8282C>T

Transcript Alleles

HGVS Amino-acid Change
NM_003126.4:c.326C>T MANE Select NP_003117.2:p.Ser109Phe
ENST00000643759.2:c.326C>T MANE Select ENSP00000495214.1:p.Ser109Phe
NM_003126.2:c.326C>T NP_003117.2:p.Ser109Phe
NM_003126.3:c.326C>T NP_003117.2:p.Ser109Phe
ENST00000368147.8:c.326C>T ENSP00000357129.4:p.Ser109Phe
ENST00000467387.1:c.132+1805C>T ENSP00000476485.1:n.132+1805C>T
ENST00000614909.4:c.326C>T ENSP00000482595.1:p.Ser109Phe
XM_011509916.1:c.326C>T XP_011508218.1:p.Ser109Phe
XM_011509916.2:c.326C>T XP_011508218.1:p.Ser109Phe
XM_011509917.1:c.326C>T XP_011508219.1:p.Ser109Phe
XM_011509917.3:c.326C>T XP_011508219.1:p.Ser109Phe
XM_011509918.1:c.326C>T XP_011508220.1:p.Ser109Phe
XM_011509918.3:c.326C>T XP_011508220.1:p.Ser109Phe
XM_011509919.1:c.326C>T XP_011508221.1:p.Ser109Phe
XM_011509919.3:c.326C>T XP_011508221.1:p.Ser109Phe
XR_921911.1:n.439C>T
XR_921911.3:n.452C>T
XR_921912.1:n.444C>T
XR_921912.2:n.454C>T