Canonical Allele Identifier: CA624212106

Gene: GALNS

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88832106G>A , CM000678.2:g.88832106G>A	GRCh38
NC_000016.9:g.88898514G>A , CM000678.1:g.88898514G>A	GRCh37
NC_000016.8:g.87426015G>A	NCBI36
NG_008667.1:g.29861C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000268695.10:c.899-5C>T MANE Select	ENSP00000268695.5:n.899-5C>T
ENST00000268695.9:c.899-5C>T	ENSP00000268695.5:n.899-5C>T
ENST00000562593.5:n.4308-5C>T
ENST00000562931.5:n.487-5C>T
ENST00000567525.5:c.580-5C>T	ENSP00000454484.1:n.580-5C>T
ENST00000568613.5:c.1018-5C>T	ENSP00000457921.1:n.1018-5C>T
NM_000512.4:c.899-5C>T	NP_000503.1:n.899-5C>T
XM_005256301.2:c.899-5C>T	XP_005256358.1:n.899-5C>T
XM_005256302.1:c.917-5C>T	XP_005256359.1:n.917-5C>T
XM_011522982.1:c.917-5C>T	XP_011521284.1:n.917-5C>T
XM_011522984.1:c.917-5C>T	XP_011521286.1:n.917-5C>T
NM_001323543.1:c.344-5C>T	NP_001310472.1:n.344-5C>T
NM_001323544.1:c.917-5C>T	NP_001310473.1:n.917-5C>T
XM_005256301.3:c.899-5C>T	XP_005256358.1:n.899-5C>T
XM_011522982.2:c.917-5C>T	XP_011521284.1:n.917-5C>T
XM_017023111.2:c.917-5C>T	XP_016878600.1:n.917-5C>T
XM_017023112.2:c.917-5C>T	XP_016878601.1:n.917-5C>T
XM_017023113.1:c.344-5C>T	XP_016878602.1:n.344-5C>T
NM_000512.5:c.899-5C>T MANE Select	NP_000503.1:n.899-5C>T
NM_001323543.2:c.344-5C>T	NP_001310472.1:n.344-5C>T
NM_001323544.2:c.917-5C>T	NP_001310473.1:n.917-5C>T