Canonical Allele Identifier: CA1446257
Gene: GALNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230243424G>A , CM000663.2:g.230243424G>A GRCh38
NC_000001.10:g.230379170G>A , CM000663.1:g.230379170G>A GRCh37
NC_000001.9:g.228445793G>A NCBI36
NG_011854.1:g.181215G>A
NG_011854.2:g.190636G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000366672.5:c.726G>A MANE Select ENSP00000355632.4:p.Ala242=
ENST00000366672.4:c.726G>A ENSP00000355632.4:p.Ala242=
ENST00000494106.1:n.689G>A
NM_001291866.1:c.612G>A NP_001278795.1:p.Ala204=
NM_004481.4:c.726G>A NP_004472.1:p.Ala242=
XM_011544154.1:c.654G>A XP_011542456.1:p.Ala218=
XM_011544155.1:c.525G>A XP_011542457.1:p.Ala175=
XM_017000963.2:c.726G>A XP_016856452.1:p.Ala242=
XM_017000964.2:c.633G>A XP_016856453.1:p.Ala211=
XM_017000965.1:c.612G>A XP_016856454.1:p.Ala204=
XM_017000966.1:c.525G>A XP_016856455.1:p.Ala175=
NM_004481.5:c.726G>A MANE Select NP_004472.1:p.Ala242=
NM_001291866.2:c.612G>A NP_001278795.1:p.Ala204=