Canonical Allele Identifier: CA343026670
Gene: SPTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.158685211T>A , CM000663.2:g.158685211T>A GRCh38
NC_000001.10:g.158655001T>A , CM000663.1:g.158655001T>A GRCh37
NC_000001.9:g.156921625T>A NCBI36
NG_011474.1:g.6506A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000643759.2:c.161A>T MANE Select ENSP00000495214.1:p.His54Leu
ENST00000368147.8:c.161A>T ENSP00000357129.4:p.His54Leu
ENST00000467387.1:c.132+29A>T ENSP00000476485.1:n.132+29A>T
ENST00000614909.4:c.161A>T ENSP00000482595.1:p.His54Leu
NM_003126.2:c.161A>T NP_003117.2:p.His54Leu
XM_011509916.1:c.161A>T XP_011508218.1:p.His54Leu
XM_011509917.1:c.161A>T XP_011508219.1:p.His54Leu
XM_011509918.1:c.161A>T XP_011508220.1:p.His54Leu
XM_011509919.1:c.161A>T XP_011508221.1:p.His54Leu
XR_921911.1:n.274A>T
XR_921912.1:n.279A>T
NM_003126.3:c.161A>T NP_003117.2:p.His54Leu
XM_011509916.2:c.161A>T XP_011508218.1:p.His54Leu
XM_011509917.3:c.161A>T XP_011508219.1:p.His54Leu
XM_011509918.3:c.161A>T XP_011508220.1:p.His54Leu
XM_011509919.3:c.161A>T XP_011508221.1:p.His54Leu
XR_921911.3:n.287A>T
XR_921912.2:n.289A>T
NM_003126.4:c.161A>T MANE Select NP_003117.2:p.His54Leu