Canonical Allele Identifier: CA1610028649

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556702T= , CM000668.2:g.10556702T=	GRCh38
NC_000006.11:g.10556935T= , CM000668.1:g.10556935T=	GRCh37
NC_000006.10:g.10664921T=	NCBI36
NG_007469.3:g.69480T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.279T= MANE Plus Clinical	ENSP00000314844.3:p.Phe93=
ENST00000397423.7:n.484+27861T=
ENST00000495262.7:c.925+26866T= MANE Select	ENSP00000419411.2:n.925+26866T=
ENST00000640968.1:c.279T=	ENSP00000492466.1:p.Phe93=
ENST00000316170.7:c.279T=	ENSP00000314844.3:p.Phe93=
ENST00000379597.7:c.925+26866T=	ENSP00000368917.3:n.925+26866T=
ENST00000397423.6:n.484+27861T=
ENST00000410107.5:c.67+47544T=	ENSP00000386321.1:n.67+47544T=
ENST00000461400.1:n.25+26866T=
ENST00000474518.1:n.508+27861T=
ENST00000475577.5:n.254+29042T=
ENST00000485764.1:n.40+26866T=
ENST00000489225.5:n.283+63771T=
ENST00000489819.5:n.175+35108T=
ENST00000495262.5:c.925+26866T=	ENSP00000419411.1:n.925+26866T=
NM_001491.2:c.279T=	NP_001482.1:p.Phe93=
NM_145649.4:c.925+26866T=	NP_663624.1:n.925+26866T=
XM_005248997.2:c.279T=	XP_005249054.1:p.Phe93=
XM_005248999.2:c.694+26866T=	XP_005249056.1:n.694+26866T=
XM_006715052.2:c.925+26866T=	XP_006715115.1:n.925+26866T=
XM_011514465.1:c.926-16428T=	XP_011512767.1:n.926-16428T=
XM_011514467.1:c.694+26866T=	XP_011512769.1:n.694+26866T=
XR_926136.1:n.1476+26866T=
XM_005248997.3:c.279T=	XP_005249054.1:p.Phe93=
XM_006715052.3:c.925+26866T=	XP_006715115.1:n.925+26866T=
XR_002956275.1:n.1476+26866T=
XR_926136.2:n.1474+26866T=
NM_001374747.1:c.925+26866T=	NP_001361676.1:n.925+26866T=
NM_001491.3:c.279T= MANE Plus Clinical	NP_001482.1:p.Phe93=
NM_145649.5:c.925+26866T= MANE Select	NP_663624.1:n.925+26866T=