Canonical Allele Identifier: CA1610027659

Gene: GCNT2

Linked Data

• dbSNP Id: rs1762684361

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556043_10556044insTTCA , CM000668.2:g.10556043_10556044insTTCA	GRCh38
NC_000006.11:g.10556276_10556277insTTCA , CM000668.1:g.10556276_10556277insTTCA	GRCh37
NC_000006.10:g.10664262_10664263insTTCA	NCBI36
NG_007469.3:g.68821_68822insTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.-381_-380insTTCA MANE Plus Clinical	ENSP00000314844.3:n.-381_-380insTTCA
ENST00000397423.7:n.484+27202_484+27203insTTCA
ENST00000495262.7:c.925+26207_925+26208insTTCA MANE Select	ENSP00000419411.2:n.925+26207_925+26208insTTCA
ENST00000316170.7:c.-381_-380insTTCA	ENSP00000314844.3:n.-381_-380insTTCA
ENST00000379597.7:c.925+26207_925+26208insTTCA	ENSP00000368917.3:n.925+26207_925+26208insTTCA
ENST00000397423.6:n.484+27202_484+27203insTTCA
ENST00000410107.5:c.67+46885_67+46886insTTCA	ENSP00000386321.1:n.67+46885_67+46886insTTCA
ENST00000461400.1:n.25+26207_25+26208insTTCA
ENST00000474518.1:n.508+27202_508+27203insTTCA
ENST00000475577.5:n.254+28383_254+28384insTTCA
ENST00000485764.1:n.40+26207_40+26208insTTCA
ENST00000489225.5:n.283+63112_283+63113insTTCA
ENST00000489819.5:n.175+34449_175+34450insTTCA
ENST00000495262.5:c.925+26207_925+26208insTTCA	ENSP00000419411.1:n.925+26207_925+26208insTTCA
NM_001491.2:c.-381_-380insTTCA	NP_001482.1:n.-381_-380insTTCA
NM_145649.4:c.925+26207_925+26208insTTCA	NP_663624.1:n.925+26207_925+26208insTTCA
XM_005248997.2:c.-381_-380insTTCA	XP_005249054.1:n.-381_-380insTTCA
XM_005248999.2:c.694+26207_694+26208insTTCA	XP_005249056.1:n.694+26207_694+26208insTTCA
XM_006715052.2:c.925+26207_925+26208insTTCA	XP_006715115.1:n.925+26207_925+26208insTTCA
XM_006715053.2:c.*85_*86insTTCA	XP_006715116.1:n.*85_*86insTTCA
XM_011514465.1:c.926-17087_926-17086insTTCA	XP_011512767.1:n.926-17087_926-17086insTTCA
XM_011514467.1:c.694+26207_694+26208insTTCA	XP_011512769.1:n.694+26207_694+26208insTTCA
XR_926136.1:n.1476+26207_1476+26208insTTCA
XM_005248997.3:c.-381_-380insTTCA	XP_005249054.1:n.-381_-380insTTCA
XM_006715052.3:c.925+26207_925+26208insTTCA	XP_006715115.1:n.925+26207_925+26208insTTCA
XR_002956275.1:n.1476+26207_1476+26208insTTCA
XR_926136.2:n.1474+26207_1474+26208insTTCA
NM_001374747.1:c.925+26207_925+26208insTTCA	NP_001361676.1:n.925+26207_925+26208insTTCA
NM_001491.3:c.-381_-380insTTCA MANE Plus Clinical	NP_001482.1:n.-381_-380insTTCA
NM_145649.5:c.925+26207_925+26208insTTCA MANE Select	NP_663624.1:n.925+26207_925+26208insTTCA