Canonical Allele Identifier: CA1610027235

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10555815G= , CM000668.2:g.10555815G=	GRCh38
NC_000006.11:g.10556048G= , CM000668.1:g.10556048G=	GRCh37
NC_000006.10:g.10664034G=	NCBI36
NG_007469.3:g.68593G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-609G= MANE Plus Clinical	ENSP00000314844.3:n.-609G=
ENST00000397423.7:n.484+26974G=
ENST00000495262.7:c.925+25979G= MANE Select	ENSP00000419411.2:n.925+25979G=
ENST00000379597.7:c.925+25979G=	ENSP00000368917.3:n.925+25979G=
ENST00000397423.6:n.484+26974G=
ENST00000410107.5:c.67+46657G=	ENSP00000386321.1:n.67+46657G=
ENST00000461400.1:n.25+25979G=
ENST00000474518.1:n.508+26974G=
ENST00000475577.5:n.254+28155G=
ENST00000485764.1:n.40+25979G=
ENST00000489225.5:n.283+62884G=
ENST00000489819.5:n.175+34221G=
ENST00000495262.5:c.925+25979G=	ENSP00000419411.1:n.925+25979G=
NM_001491.2:c.-609G=	NP_001482.1:n.-609G=
NM_145649.4:c.925+25979G=	NP_663624.1:n.925+25979G=
XM_005248999.2:c.694+25979G=	XP_005249056.1:n.694+25979G=
XM_006715052.2:c.925+25979G=	XP_006715115.1:n.925+25979G=
XM_006715053.2:c.926-19G=	XP_006715116.1:n.926-19G=
XM_011514465.1:c.926-17315G=	XP_011512767.1:n.926-17315G=
XM_011514467.1:c.694+25979G=	XP_011512769.1:n.694+25979G=
XR_926136.1:n.1476+25979G=
XM_006715052.3:c.925+25979G=	XP_006715115.1:n.925+25979G=
XR_002956275.1:n.1476+25979G=
XR_926136.2:n.1474+25979G=
NM_001374747.1:c.925+25979G=	NP_001361676.1:n.925+25979G=
NM_001491.3:c.-609G= MANE Plus Clinical	NP_001482.1:n.-609G=
NM_145649.5:c.925+25979G= MANE Select	NP_663624.1:n.925+25979G=