Canonical Allele Identifier: CA2241322188

Gene: GALNS

Linked Data

• dbSNP Id: rs1911551234

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88831974del , CM000678.2:g.88831974del	GRCh38
NC_000016.9:g.88898382del , CM000678.1:g.88898382del	GRCh37
NC_000016.8:g.87425883del	NCBI36
NG_008667.1:g.29994del

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.1002+25del MANE Select	ENSP00000268695.5:n.1002+25del
ENST00000268695.9:c.1002+25del	ENSP00000268695.5:n.1002+25del
ENST00000562593.5:n.4411+25del
ENST00000567525.5:c.683+25del	ENSP00000454484.1:n.683+25del
ENST00000568613.5:c.1121+25del	ENSP00000457921.1:n.1121+25del
NM_000512.4:c.1002+25del	NP_000503.1:n.1002+25del
XM_005256301.2:c.1002+25del	XP_005256358.1:n.1002+25del
XM_005256302.1:c.1020+25del	XP_005256359.1:n.1020+25del
XM_011522982.1:c.1020+25del	XP_011521284.1:n.1020+25del
XM_011522984.1:c.1020+25del	XP_011521286.1:n.1020+25del
NM_001323543.1:c.447+25del	NP_001310472.1:n.447+25del
NM_001323544.1:c.1020+25del	NP_001310473.1:n.1020+25del
XM_005256301.3:c.1002+25del	XP_005256358.1:n.1002+25del
XM_011522982.2:c.1020+25del	XP_011521284.1:n.1020+25del
XM_017023111.2:c.1020+25del	XP_016878600.1:n.1020+25del
XM_017023112.2:c.1020+25del	XP_016878601.1:n.1020+25del
XM_017023113.1:c.447+25del	XP_016878602.1:n.447+25del
NM_000512.5:c.1002+25del MANE Select	NP_000503.1:n.1002+25del
NM_001323543.2:c.447+25del	NP_001310472.1:n.447+25del
NM_001323544.2:c.1020+25del	NP_001310473.1:n.1020+25del