Canonical Allele Identifier: CA1610027544

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10555977C= , CM000668.2:g.10555977C=	GRCh38
NC_000006.11:g.10556210C= , CM000668.1:g.10556210C=	GRCh37
NC_000006.10:g.10664196C=	NCBI36
NG_007469.3:g.68755C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-447C= MANE Plus Clinical	ENSP00000314844.3:n.-447C=
ENST00000397423.7:n.484+27136C=
ENST00000495262.7:c.925+26141C= MANE Select	ENSP00000419411.2:n.925+26141C=
ENST00000379597.7:c.925+26141C=	ENSP00000368917.3:n.925+26141C=
ENST00000397423.6:n.484+27136C=
ENST00000410107.5:c.67+46819C=	ENSP00000386321.1:n.67+46819C=
ENST00000461400.1:n.25+26141C=
ENST00000474518.1:n.508+27136C=
ENST00000475577.5:n.254+28317C=
ENST00000485764.1:n.40+26141C=
ENST00000489225.5:n.283+63046C=
ENST00000489819.5:n.175+34383C=
ENST00000495262.5:c.925+26141C=	ENSP00000419411.1:n.925+26141C=
NM_001491.2:c.-447C=	NP_001482.1:n.-447C=
NM_145649.4:c.925+26141C=	NP_663624.1:n.925+26141C=
XM_005248999.2:c.694+26141C=	XP_005249056.1:n.694+26141C=
XM_006715052.2:c.925+26141C=	XP_006715115.1:n.925+26141C=
XM_006715053.2:c.*19C=	XP_006715116.1:n.*19C=
XM_011514465.1:c.926-17153C=	XP_011512767.1:n.926-17153C=
XM_011514467.1:c.694+26141C=	XP_011512769.1:n.694+26141C=
XR_926136.1:n.1476+26141C=
XM_006715052.3:c.925+26141C=	XP_006715115.1:n.925+26141C=
XR_002956275.1:n.1476+26141C=
XR_926136.2:n.1474+26141C=
NM_001374747.1:c.925+26141C=	NP_001361676.1:n.925+26141C=
NM_001491.3:c.-447C= MANE Plus Clinical	NP_001482.1:n.-447C=
NM_145649.5:c.925+26141C= MANE Select	NP_663624.1:n.925+26141C=