Canonical Allele Identifier: CA397101430
Community Standard Title: NM_000512.5(GALNS):c.922T>C (p.Cys308Arg)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88832078A>G , CM000678.2:g.88832078A>G GRCh38
NC_000016.9:g.88898486A>G , CM000678.1:g.88898486A>G GRCh37
NC_000016.8:g.87425987A>G NCBI36
NG_008667.1:g.29889T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.922T>C MANE Select NP_000503.1:p.Cys308Arg
ENST00000268695.10:c.922T>C MANE Select ENSP00000268695.5:p.Cys308Arg
NM_000512.4:c.922T>C NP_000503.1:p.Cys308Arg
NM_001323543.1:c.367T>C NP_001310472.1:p.Cys123Arg
NM_001323543.2:c.367T>C NP_001310472.1:p.Cys123Arg
NM_001323544.1:c.940T>C NP_001310473.1:p.Cys314Arg
NM_001323544.2:c.940T>C NP_001310473.1:p.Cys314Arg
ENST00000268695.9:c.922T>C ENSP00000268695.5:p.Cys308Arg
ENST00000562593.5:n.4331T>C
ENST00000562931.5:n.510T>C
ENST00000567525.5:c.603T>C ENSP00000454484.1:n.603T>C
ENST00000568613.5:c.1041T>C ENSP00000457921.1:n.1041T>C
XM_005256301.2:c.922T>C XP_005256358.1:p.Cys308Arg
XM_005256301.3:c.922T>C XP_005256358.1:p.Cys308Arg
XM_005256302.1:c.940T>C XP_005256359.1:p.Cys314Arg
XM_011522982.1:c.940T>C XP_011521284.1:p.Cys314Arg
XM_011522982.2:c.940T>C XP_011521284.1:p.Cys314Arg
XM_011522984.1:c.940T>C XP_011521286.1:p.Cys314Arg
XM_017023111.2:c.940T>C XP_016878600.1:p.Cys314Arg
XM_017023112.2:c.940T>C XP_016878601.1:p.Cys314Arg
XM_017023113.1:c.367T>C XP_016878602.1:p.Cys123Arg