Canonical Allele Identifier: CA343025392
Gene: SPTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158685137T>C , CM000663.2:g.158685137T>C GRCh38
NC_000001.10:g.158654927T>C , CM000663.1:g.158654927T>C GRCh37
NC_000001.9:g.156921551T>C NCBI36
NG_011474.1:g.6580A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000643759.2:c.235A>G MANE Select ENSP00000495214.1:p.Lys79Glu
ENST00000368147.8:c.235A>G ENSP00000357129.4:p.Lys79Glu
ENST00000467387.1:c.132+103A>G ENSP00000476485.1:n.132+103A>G
ENST00000614909.4:c.235A>G ENSP00000482595.1:p.Lys79Glu
NM_003126.2:c.235A>G NP_003117.2:p.Lys79Glu
XM_011509916.1:c.235A>G XP_011508218.1:p.Lys79Glu
XM_011509917.1:c.235A>G XP_011508219.1:p.Lys79Glu
XM_011509918.1:c.235A>G XP_011508220.1:p.Lys79Glu
XM_011509919.1:c.235A>G XP_011508221.1:p.Lys79Glu
XR_921911.1:n.348A>G
XR_921912.1:n.353A>G
NM_003126.3:c.235A>G NP_003117.2:p.Lys79Glu
XM_011509916.2:c.235A>G XP_011508218.1:p.Lys79Glu
XM_011509917.3:c.235A>G XP_011508219.1:p.Lys79Glu
XM_011509918.3:c.235A>G XP_011508220.1:p.Lys79Glu
XM_011509919.3:c.235A>G XP_011508221.1:p.Lys79Glu
XR_921911.3:n.361A>G
XR_921912.2:n.363A>G
NM_003126.4:c.235A>G MANE Select NP_003117.2:p.Lys79Glu