Canonical Allele Identifier: CA1610027775

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556100_10556102delinsAAG , CM000668.2:g.10556100_10556102delinsAAG	GRCh38
NC_000006.11:g.10556333_10556335delinsAAG , CM000668.1:g.10556333_10556335delinsAAG	GRCh37
NC_000006.10:g.10664319_10664321delinsAAG	NCBI36
NG_007469.3:g.68878_68880delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-324_-322delinsAAG MANE Plus Clinical	ENSP00000314844.3:n.-324_-322delinsAAG
ENST00000397423.7:n.484+27259_484+27261delinsAAG
ENST00000495262.7:c.925+26264_925+26266delinsAAG MANE Select	ENSP00000419411.2:n.925+26264_925+26266delinsAAG
ENST00000316170.7:c.-324_-322delinsAAG	ENSP00000314844.3:n.-324_-322delinsAAG
ENST00000379597.7:c.925+26264_925+26266delinsAAG	ENSP00000368917.3:n.925+26264_925+26266delinsAAG
ENST00000397423.6:n.484+27259_484+27261delinsAAG
ENST00000410107.5:c.67+46942_67+46944delinsAAG	ENSP00000386321.1:n.67+46942_67+46944delinsAAG
ENST00000461400.1:n.25+26264_25+26266delinsAAG
ENST00000474518.1:n.508+27259_508+27261delinsAAG
ENST00000475577.5:n.254+28440_254+28442delinsAAG
ENST00000485764.1:n.40+26264_40+26266delinsAAG
ENST00000489225.5:n.283+63169_283+63171delinsAAG
ENST00000489819.5:n.175+34506_175+34508delinsAAG
ENST00000495262.5:c.925+26264_925+26266delinsAAG	ENSP00000419411.1:n.925+26264_925+26266delinsAAG
NM_001491.2:c.-324_-322delinsAAG	NP_001482.1:n.-324_-322delinsAAG
NM_145649.4:c.925+26264_925+26266delinsAAG	NP_663624.1:n.925+26264_925+26266delinsAAG
XM_005248997.2:c.-324_-322delinsAAG	XP_005249054.1:n.-324_-322delinsAAG
XM_005248999.2:c.694+26264_694+26266delinsAAG	XP_005249056.1:n.694+26264_694+26266delinsAAG
XM_006715052.2:c.925+26264_925+26266delinsAAG	XP_006715115.1:n.925+26264_925+26266delinsAAG
XM_006715053.2:c.*142_*144delinsAAG	XP_006715116.1:n.*142_*144delinsAAG
XM_011514465.1:c.926-17030_926-17028delinsAAG	XP_011512767.1:n.926-17030_926-17028delinsAAG
XM_011514467.1:c.694+26264_694+26266delinsAAG	XP_011512769.1:n.694+26264_694+26266delinsAAG
XR_926136.1:n.1476+26264_1476+26266delinsAAG
XM_005248997.3:c.-324_-322delinsAAG	XP_005249054.1:n.-324_-322delinsAAG
XM_006715052.3:c.925+26264_925+26266delinsAAG	XP_006715115.1:n.925+26264_925+26266delinsAAG
XR_002956275.1:n.1476+26264_1476+26266delinsAAG
XR_926136.2:n.1474+26264_1474+26266delinsAAG
NM_001374747.1:c.925+26264_925+26266delinsAAG	NP_001361676.1:n.925+26264_925+26266delinsAAG
NM_001491.3:c.-324_-322delinsAAG MANE Plus Clinical	NP_001482.1:n.-324_-322delinsAAG
NM_145649.5:c.925+26264_925+26266delinsAAG MANE Select	NP_663624.1:n.925+26264_925+26266delinsAAG