Canonical Allele Identifier: CA397098158

Gene: GALNS

Linked Data

• gnomAD v4: 16-88826714-C-G
• MyVariant Identifiers: chr16:g.88893122C>G (hg19) ; chr16:g.88826714C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88826714C>G , CM000678.2:g.88826714C>G	GRCh38
NC_000016.9:g.88893122C>G , CM000678.1:g.88893122C>G	GRCh37
NC_000016.8:g.87420623C>G	NCBI36
NG_008667.1:g.35253G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.1127G>C MANE Select	ENSP00000268695.5:p.Arg376Pro
ENST00000268695.9:c.1127G>C	ENSP00000268695.5:p.Arg376Pro
ENST00000562593.5:n.4536G>C
ENST00000564263.1:n.403G>C
ENST00000567525.5:c.808G>C	ENSP00000454484.1:n.808G>C
ENST00000568613.5:c.1246G>C	ENSP00000457921.1:n.1246G>C
NM_000512.4:c.1127G>C	NP_000503.1:p.Arg376Pro
XM_005256301.2:c.1127G>C	XP_005256358.1:p.Arg376Pro
XM_005256302.1:c.1145G>C	XP_005256359.1:p.Arg382Pro
XM_011522982.1:c.1145G>C	XP_011521284.1:p.Arg382Pro
XM_011522984.1:c.1145G>C	XP_011521286.1:p.Arg382Pro
NM_001323543.1:c.572G>C	NP_001310472.1:p.Arg191Pro
NM_001323544.1:c.1145G>C	NP_001310473.1:p.Arg382Pro
XM_005256301.3:c.1127G>C	XP_005256358.1:p.Arg376Pro
XM_011522982.2:c.1145G>C	XP_011521284.1:p.Arg382Pro
XM_017023111.2:c.1145G>C	XP_016878600.1:p.Arg382Pro
XM_017023112.2:c.1145G>C	XP_016878601.1:p.Arg382Pro
XM_017023113.1:c.572G>C	XP_016878602.1:p.Arg191Pro
NM_000512.5:c.1127G>C MANE Select	NP_000503.1:p.Arg376Pro
NM_001323543.2:c.572G>C	NP_001310472.1:p.Arg191Pro
NM_001323544.2:c.1145G>C	NP_001310473.1:p.Arg382Pro