Canonical Allele Identifier: CA1446091

Gene: GALNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230203300C>G , CM000663.2:g.230203300C>G	GRCh38
NC_000001.10:g.230339046C>G , CM000663.1:g.230339046C>G	GRCh37
NC_000001.9:g.228405669C>G	NCBI36
NG_011854.1:g.141091C>G
NG_011854.2:g.150512C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004481.5:c.374+10C>G MANE Select	NP_004472.1:n.374+10C>G
ENST00000366672.5:c.374+10C>G MANE Select	ENSP00000355632.4:n.374+10C>G
NM_001291866.1:c.260+10C>G	NP_001278795.1:n.260+10C>G
NM_001291866.2:c.260+10C>G	NP_001278795.1:n.260+10C>G
NM_004481.4:c.374+10C>G	NP_004472.1:n.374+10C>G
ENST00000366672.4:c.374+10C>G	ENSP00000355632.4:n.374+10C>G
ENST00000494106.1:n.337+10C>G
XM_011544154.1:c.302+10C>G	XP_011542456.1:n.302+10C>G
XM_011544155.1:c.173+10C>G	XP_011542457.1:n.173+10C>G
XM_017000963.2:c.374+10C>G	XP_016856452.1:n.374+10C>G
XM_017000964.2:c.281+10C>G	XP_016856453.1:n.281+10C>G
XM_017000965.1:c.260+10C>G	XP_016856454.1:n.260+10C>G
XM_017000966.1:c.173+10C>G	XP_016856455.1:n.173+10C>G