Canonical Allele Identifier: CA8234885
Community Standard Title: NM_000512.5(GALNS):c.986A>C (p.His329Pro)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88832014T>G , CM000678.2:g.88832014T>G GRCh38
NC_000016.9:g.88898422T>G , CM000678.1:g.88898422T>G GRCh37
NC_000016.8:g.87425923T>G NCBI36
NG_008667.1:g.29953A>C

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.986A>C MANE Select NP_000503.1:p.His329Pro
ENST00000268695.10:c.986A>C MANE Select ENSP00000268695.5:p.His329Pro
NM_000512.4:c.986A>C NP_000503.1:p.His329Pro
NM_001323543.1:c.431A>C NP_001310472.1:p.His144Pro
NM_001323543.2:c.431A>C NP_001310472.1:p.His144Pro
NM_001323544.1:c.1004A>C NP_001310473.1:p.His335Pro
NM_001323544.2:c.1004A>C NP_001310473.1:p.His335Pro
ENST00000268695.9:c.986A>C ENSP00000268695.5:p.His329Pro
ENST00000562593.5:n.4395A>C
ENST00000567525.5:c.667A>C ENSP00000454484.1:n.667A>C
ENST00000568613.5:c.1105A>C ENSP00000457921.1:n.1105A>C
XM_005256301.2:c.986A>C XP_005256358.1:p.His329Pro
XM_005256301.3:c.986A>C XP_005256358.1:p.His329Pro
XM_005256302.1:c.1004A>C XP_005256359.1:p.His335Pro
XM_011522982.1:c.1004A>C XP_011521284.1:p.His335Pro
XM_011522982.2:c.1004A>C XP_011521284.1:p.His335Pro
XM_011522984.1:c.1004A>C XP_011521286.1:p.His335Pro
XM_017023111.2:c.1004A>C XP_016878600.1:p.His335Pro
XM_017023112.2:c.1004A>C XP_016878601.1:p.His335Pro
XM_017023113.1:c.431A>C XP_016878602.1:p.His144Pro