Canonical Allele Identifier: CA343020603
Gene: SPTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158680632T>C , CM000663.2:g.158680632T>C GRCh38
NC_000001.10:g.158650422T>C , CM000663.1:g.158650422T>C GRCh37
NC_000001.9:g.156917046T>C NCBI36
NG_011474.1:g.11085A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000643759.2:c.629A>G MANE Select ENSP00000495214.1:p.Lys210Arg
ENST00000368147.8:c.629A>G ENSP00000357129.4:p.Lys210Arg
ENST00000467387.1:c.133-2098A>G ENSP00000476485.1:n.133-2098A>G
ENST00000614909.4:c.629A>G ENSP00000482595.1:p.Lys210Arg
NM_003126.2:c.629A>G NP_003117.2:p.Lys210Arg
XM_011509916.1:c.629A>G XP_011508218.1:p.Lys210Arg
XM_011509917.1:c.629A>G XP_011508219.1:p.Lys210Arg
XM_011509918.1:c.629A>G XP_011508220.1:p.Lys210Arg
XM_011509919.1:c.629A>G XP_011508221.1:p.Lys210Arg
XR_921911.1:n.742A>G
XR_921912.1:n.747A>G
NM_003126.3:c.629A>G NP_003117.2:p.Lys210Arg
XM_011509916.2:c.629A>G XP_011508218.1:p.Lys210Arg
XM_011509917.3:c.629A>G XP_011508219.1:p.Lys210Arg
XM_011509918.3:c.629A>G XP_011508220.1:p.Lys210Arg
XM_011509919.3:c.629A>G XP_011508221.1:p.Lys210Arg
XR_921911.3:n.755A>G
XR_921912.2:n.757A>G
NM_003126.4:c.629A>G MANE Select NP_003117.2:p.Lys210Arg