Canonical Allele Identifier: CA10621048

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10626688G>A , CM000668.2:g.10626688G>A	GRCh38
NC_000006.11:g.10626921G>A , CM000668.1:g.10626921G>A	GRCh37
NC_000006.10:g.10734907G>A	NCBI36
NG_007469.3:g.139466G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265012.5:c.*81G>A	ENSP00000265012.4:n.*81G>A
ENST00000316170.9:c.*81G>A MANE Plus Clinical	ENSP00000314844.3:n.*81G>A
ENST00000397423.7:n.849G>A
ENST00000495262.7:c.*81G>A MANE Select	ENSP00000419411.2:n.*81G>A
ENST00000265012.4:c.*81G>A	ENSP00000265012.4:n.*81G>A
ENST00000316170.7:c.*81G>A	ENSP00000314844.3:n.*81G>A
ENST00000379597.7:c.*81G>A	ENSP00000368917.3:n.*81G>A
ENST00000397423.6:n.849G>A
ENST00000410107.5:c.*81G>A	ENSP00000386321.1:n.*81G>A
ENST00000489225.5:n.648G>A
ENST00000495262.5:c.*81G>A	ENSP00000419411.1:n.*81G>A
NM_001491.2:c.*81G>A	NP_001482.1:n.*81G>A
NM_145649.4:c.*81G>A	NP_663624.1:n.*81G>A
NM_145655.3:c.*81G>A	NP_663630.2:n.*81G>A
XM_005248999.2:c.*81G>A	XP_005249056.1:n.*81G>A
XM_006715052.2:c.*81G>A	XP_006715115.1:n.*81G>A
XM_011514467.1:c.*81G>A	XP_011512769.1:n.*81G>A
XM_006715052.3:c.*81G>A	XP_006715115.1:n.*81G>A
NM_001374747.1:c.*81G>A	NP_001361676.1:n.*81G>A
NM_001491.3:c.*81G>A MANE Plus Clinical	NP_001482.1:n.*81G>A
NM_145649.5:c.*81G>A MANE Select	NP_663624.1:n.*81G>A
NM_145655.4:c.*81G>A	NP_663630.2:n.*81G>A