Canonical Allele Identifier: CA8234978

Gene: GALNS

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.88835340G>A , CM000678.2:g.88835340G>A	GRCh38
NC_000016.9:g.88901748G>A , CM000678.1:g.88901748G>A	GRCh37
NC_000016.8:g.87429249G>A	NCBI36
NG_008667.1:g.26627C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000512.5:c.771C>T MANE Select	NP_000503.1:p.Ala257=
ENST00000268695.10:c.771C>T MANE Select	ENSP00000268695.5:p.Ala257=
NM_000512.4:c.771C>T	NP_000503.1:p.Ala257=
NM_001323543.1:c.216C>T	NP_001310472.1:p.Ala72=
NM_001323543.2:c.216C>T	NP_001310472.1:p.Ala72=
NM_001323544.1:c.789C>T	NP_001310473.1:p.Ala263=
NM_001323544.2:c.789C>T	NP_001310473.1:p.Ala263=
ENST00000268695.9:c.771C>T	ENSP00000268695.5:p.Ala257=
ENST00000562593.5:n.4180C>T
ENST00000562931.5:n.359C>T
ENST00000567525.5:c.452C>T	ENSP00000454484.1:n.452C>T
ENST00000568613.5:c.890C>T	ENSP00000457921.1:n.890C>T
XM_005256301.2:c.771C>T	XP_005256358.1:p.Ala257=
XM_005256301.3:c.771C>T	XP_005256358.1:p.Ala257=
XM_005256302.1:c.789C>T	XP_005256359.1:p.Ala263=
XM_011522982.1:c.789C>T	XP_011521284.1:p.Ala263=
XM_011522982.2:c.789C>T	XP_011521284.1:p.Ala263=
XM_011522984.1:c.789C>T	XP_011521286.1:p.Ala263=
XM_017023111.2:c.789C>T	XP_016878600.1:p.Ala263=
XM_017023112.2:c.789C>T	XP_016878601.1:p.Ala263=
XM_017023113.1:c.216C>T	XP_016878602.1:p.Ala72=