Canonical Allele Identifier: CA134081103

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10585747A>G , CM000668.2:g.10585747A>G	GRCh38
NC_000006.11:g.10585980A>G , CM000668.1:g.10585980A>G	GRCh37
NC_000006.10:g.10693966A>G	NCBI36
NG_007469.3:g.98525A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_145649.5:c.926-35604A>G MANE Select	NP_663624.1:n.926-35604A>G
ENST00000495262.7:c.926-35604A>G MANE Select	ENSP00000419411.2:n.926-35604A>G
NM_001491.3:c.919+28405A>G MANE Plus Clinical	NP_001482.1:n.919+28405A>G
ENST00000316170.9:c.919+28405A>G MANE Plus Clinical	ENSP00000314844.3:n.919+28405A>G
NM_001374747.1:c.926-35604A>G	NP_001361676.1:n.926-35604A>G
NM_001491.2:c.919+28405A>G	NP_001482.1:n.919+28405A>G
NM_145649.4:c.926-35604A>G	NP_663624.1:n.926-35604A>G
ENST00000265012.4:c.-243A>G	ENSP00000265012.4:n.-243A>G
ENST00000316170.7:c.919+28405A>G	ENSP00000314844.3:n.919+28405A>G
ENST00000379597.7:c.926-35604A>G	ENSP00000368917.3:n.926-35604A>G
ENST00000397423.6:n.485-35604A>G
ENST00000397423.7:n.485-35604A>G
ENST00000410107.5:c.68-35604A>G	ENSP00000386321.1:n.68-35604A>G
ENST00000459872.1:n.542+28405A>G
ENST00000461400.1:n.26-35604A>G
ENST00000474518.1:n.509-35604A>G
ENST00000475577.5:n.255-35604A>G
ENST00000485764.1:n.41-33458A>G
ENST00000489225.5:n.284-35604A>G
ENST00000489819.5:n.176-35604A>G
ENST00000495262.5:c.926-35604A>G	ENSP00000419411.1:n.926-35604A>G
XM_005248999.2:c.695-35604A>G	XP_005249056.1:n.695-35604A>G
XM_006715052.2:c.926-35604A>G	XP_006715115.1:n.926-35604A>G
XM_006715052.3:c.926-35604A>G	XP_006715115.1:n.926-35604A>G
XM_011514466.1:c.-243A>G	XP_011512768.1:n.-243A>G
XM_011514467.1:c.695-35604A>G	XP_011512769.1:n.695-35604A>G
XR_002956275.1:n.1477-15578A>G
XR_926136.1:n.1477-34118A>G
XR_926136.2:n.1475-34118A>G
XR_926137.1:n.432A>G
XR_926138.1:n.432A>G