Canonical Allele Identifier: CA8235027
Community Standard Title: NM_000512.5(GALNS):c.697G>A (p.Asp233Asn)
Gene: GALNS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.88835786C>T , CM000678.2:g.88835786C>T GRCh38
NC_000016.9:g.88902194C>T , CM000678.1:g.88902194C>T GRCh37
NC_000016.8:g.87429695C>T NCBI36
NG_008667.1:g.26181G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000512.5:c.697G>A MANE Select NP_000503.1:p.Asp233Asn
ENST00000268695.10:c.697G>A MANE Select ENSP00000268695.5:p.Asp233Asn
NM_000512.4:c.697G>A NP_000503.1:p.Asp233Asn
NM_001323543.1:c.142G>A NP_001310472.1:p.Asp48Asn
NM_001323543.2:c.142G>A NP_001310472.1:p.Asp48Asn
NM_001323544.1:c.715G>A NP_001310473.1:p.Asp239Asn
NM_001323544.2:c.715G>A NP_001310473.1:p.Asp239Asn
ENST00000268695.9:c.697G>A ENSP00000268695.5:p.Asp233Asn
ENST00000562593.5:n.4106G>A
ENST00000562831.1:c.481G>A ENSP00000455174.1:p.Asp161Asn
ENST00000562931.5:n.285G>A
ENST00000566563.1:n.399G>A
ENST00000567525.5:c.378G>A ENSP00000454484.1:n.378G>A
ENST00000568613.5:c.816G>A ENSP00000457921.1:n.816G>A
XM_005256301.2:c.697G>A XP_005256358.1:p.Asp233Asn
XM_005256301.3:c.697G>A XP_005256358.1:p.Asp233Asn
XM_005256302.1:c.715G>A XP_005256359.1:p.Asp239Asn
XM_011522982.1:c.715G>A XP_011521284.1:p.Asp239Asn
XM_011522982.2:c.715G>A XP_011521284.1:p.Asp239Asn
XM_011522984.1:c.715G>A XP_011521286.1:p.Asp239Asn
XM_017023111.2:c.715G>A XP_016878600.1:p.Asp239Asn
XM_017023112.2:c.715G>A XP_016878601.1:p.Asp239Asn
XM_017023113.1:c.142G>A XP_016878602.1:p.Asp48Asn