Canonical Allele Identifier: CA397081190

Gene: GALNS

Linked Data

• MyVariant Identifiers: chr16:g.88902632T>C (hg19) ; chr16:g.88836224T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88836224T>C , CM000678.2:g.88836224T>C	GRCh38
NC_000016.9:g.88902632T>C , CM000678.1:g.88902632T>C	GRCh37
NC_000016.8:g.87430133T>C	NCBI36
NG_008667.1:g.25743A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.610A>G MANE Select	ENSP00000268695.5:p.Asn204Asp
ENST00000268695.9:c.610A>G	ENSP00000268695.5:p.Asn204Asp
ENST00000562593.5:n.4019A>G
ENST00000562831.1:c.394A>G	ENSP00000455174.1:p.Asn132Asp
ENST00000562931.5:n.198A>G
ENST00000566563.1:n.312A>G
ENST00000567525.5:c.291A>G	ENSP00000454484.1:n.291A>G
ENST00000568613.5:c.729A>G	ENSP00000457921.1:n.729A>G
NM_000512.4:c.610A>G	NP_000503.1:p.Asn204Asp
XM_005256301.2:c.610A>G	XP_005256358.1:p.Asn204Asp
XM_005256302.1:c.628A>G	XP_005256359.1:p.Asn210Asp
XM_011522982.1:c.628A>G	XP_011521284.1:p.Asn210Asp
XM_011522984.1:c.628A>G	XP_011521286.1:p.Asn210Asp
NM_001323543.1:c.55A>G	NP_001310472.1:p.Asn19Asp
NM_001323544.1:c.628A>G	NP_001310473.1:p.Asn210Asp
XM_005256301.3:c.610A>G	XP_005256358.1:p.Asn204Asp
XM_011522982.2:c.628A>G	XP_011521284.1:p.Asn210Asp
XM_017023111.2:c.628A>G	XP_016878600.1:p.Asn210Asp
XM_017023112.2:c.628A>G	XP_016878601.1:p.Asn210Asp
XM_017023113.1:c.55A>G	XP_016878602.1:p.Asn19Asp
NM_000512.5:c.610A>G MANE Select	NP_000503.1:p.Asn204Asp
NM_001323543.2:c.55A>G	NP_001310472.1:p.Asn19Asp
NM_001323544.2:c.628A>G	NP_001310473.1:p.Asn210Asp