Canonical Allele Identifier: CA1226438138

Gene: GALNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.230169259G= , CM000663.2:g.230169259G=	GRCh38
NC_000001.10:g.230305005G= , CM000663.1:g.230305005G=	GRCh37
NC_000001.9:g.228371628G=	NCBI36
NG_011854.1:g.107050G=
NG_011854.2:g.116471G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000366672.5:c.127-8959G= MANE Select	ENSP00000355632.4:n.127-8959G=
ENST00000366672.4:c.127-8959G=	ENSP00000355632.4:n.127-8959G=
ENST00000494106.1:n.90-8959G=
NM_001291866.1:c.13-8959G=	NP_001278795.1:n.13-8959G=
NM_004481.4:c.127-8959G=	NP_004472.1:n.127-8959G=
XM_011544154.1:c.55-8959G=	XP_011542456.1:n.55-8959G=
XM_011544155.1:c.-75-8959G=	XP_011542457.1:n.-75-8959G=
XM_017000963.2:c.127-8959G=	XP_016856452.1:n.127-8959G=
XM_017000964.2:c.34-8959G=	XP_016856453.1:n.34-8959G=
XM_017000965.1:c.13-8959G=	XP_016856454.1:n.13-8959G=
XM_017000966.1:c.-75-8959G=	XP_016856455.1:n.-75-8959G=
NM_004481.5:c.127-8959G= MANE Select	NP_004472.1:n.127-8959G=
NM_001291866.2:c.13-8959G=	NP_001278795.1:n.13-8959G=