Canonical Allele Identifier: CA397094123

Gene: GALNS

Linked Data

• gnomAD v4: 16-88818020-T-G
• MyVariant Identifiers: chr16:g.88884428T>G (hg19) ; chr16:g.88818020T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88818020T>G , CM000678.2:g.88818020T>G	GRCh38
NC_000016.9:g.88884428T>G , CM000678.1:g.88884428T>G	GRCh37
NC_000016.8:g.87411929T>G	NCBI36
NG_008667.1:g.43947A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.1469A>C MANE Select	ENSP00000268695.5:p.Asn490Thr
ENST00000268695.9:c.1469A>C	ENSP00000268695.5:p.Asn490Thr
ENST00000562593.5:n.4878A>C
ENST00000567525.5:c.1150A>C	ENSP00000454484.1:n.1150A>C
ENST00000568613.5:c.1588A>C	ENSP00000457921.1:n.1588A>C
NM_000512.4:c.1469A>C	NP_000503.1:p.Asn490Thr
XM_005256301.2:c.1469A>C	XP_005256358.1:p.Asn490Thr
XM_005256302.1:c.1487A>C	XP_005256359.1:p.Asn496Thr
XM_011522982.1:c.1487A>C	XP_011521284.1:p.Asn496Thr
XM_011522984.1:c.1487A>C	XP_011521286.1:p.Asn496Thr
NM_001323543.1:c.914A>C	NP_001310472.1:p.Asn305Thr
NM_001323544.1:c.1487A>C	NP_001310473.1:p.Asn496Thr
XM_005256301.3:c.1469A>C	XP_005256358.1:p.Asn490Thr
XM_011522982.2:c.1487A>C	XP_011521284.1:p.Asn496Thr
XM_017023111.2:c.1487A>C	XP_016878600.1:p.Asn496Thr
XM_017023112.2:c.1487A>C	XP_016878601.1:p.Asn496Thr
XM_017023113.1:c.914A>C	XP_016878602.1:p.Asn305Thr
NM_000512.5:c.1469A>C MANE Select	NP_000503.1:p.Asn490Thr
NM_001323543.2:c.914A>C	NP_001310472.1:p.Asn305Thr
NM_001323544.2:c.1487A>C	NP_001310473.1:p.Asn496Thr