Canonical Allele Identifier: CA2634895336

Gene: GALNS

Linked Data

• gnomAD v4: 16-88840916-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88840918del , CM000678.2:g.88840918del	GRCh38
NC_000016.9:g.88907326del , CM000678.1:g.88907326del	GRCh37
NC_000016.8:g.87434827del	NCBI36
NG_008667.1:g.21050del

Transcript Alleles

HGVS	Amino-acid change
ENST00000268695.10:c.422+75del MANE Select	ENSP00000268695.5:n.422+75del
ENST00000268695.9:c.422+75del	ENSP00000268695.5:n.422+75del
ENST00000562593.5:n.3831+75del
ENST00000562831.1:c.206+75del	ENSP00000455174.1:n.206+75del
ENST00000565364.1:n.558-65del
ENST00000567525.5:c.247+75del	ENSP00000454484.1:n.247+75del
ENST00000567779.1:n.327del
ENST00000568613.5:c.541+75del	ENSP00000457921.1:n.541+75del
NM_000512.4:c.422+75del	NP_000503.1:n.422+75del
XM_005256301.2:c.422+75del	XP_005256358.1:n.422+75del
XM_005256302.1:c.440+75del	XP_005256359.1:n.440+75del
XM_011522982.1:c.440+75del	XP_011521284.1:n.440+75del
XM_011522984.1:c.440+75del	XP_011521286.1:n.440+75del
NM_001323543.1:c.-134+75del	NP_001310472.1:n.-134+75del
NM_001323544.1:c.440+75del	NP_001310473.1:n.440+75del
XM_005256301.3:c.422+75del	XP_005256358.1:n.422+75del
XM_011522982.2:c.440+75del	XP_011521284.1:n.440+75del
XM_017023111.2:c.440+75del	XP_016878600.1:n.440+75del
XM_017023112.2:c.440+75del	XP_016878601.1:n.440+75del
XM_017023113.1:c.-134+75del	XP_016878602.1:n.-134+75del
NM_000512.5:c.422+75del MANE Select	NP_000503.1:n.422+75del
NM_001323543.2:c.-134+75del	NP_001310472.1:n.-134+75del
NM_001323544.2:c.440+75del	NP_001310473.1:n.440+75del