Canonical Allele Identifier: CA1610028556

Gene: GCNT2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556630_10556633delinsGTCT , CM000668.2:g.10556630_10556633delinsGTCT	GRCh38
NC_000006.11:g.10556863_10556866delinsGTCT , CM000668.1:g.10556863_10556866delinsGTCT	GRCh37
NC_000006.10:g.10664849_10664852delinsGTCT	NCBI36
NG_007469.3:g.69408_69411delinsGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.207_210delinsGTCT MANE Plus Clinical	ENSP00000314844.3:p.Lys69=
ENST00000397423.7:n.484+27789_484+27792delinsGTCT
ENST00000495262.7:c.925+26794_925+26797delinsGTCT MANE Select	ENSP00000419411.2:n.925+26794_925+26797delinsGTCT
ENST00000640968.1:c.207_210delinsGTCT	ENSP00000492466.1:p.Lys69=
ENST00000316170.7:c.207_210delinsGTCT	ENSP00000314844.3:p.Lys69=
ENST00000379597.7:c.925+26794_925+26797delinsGTCT	ENSP00000368917.3:n.925+26794_925+26797delinsGTCT
ENST00000397423.6:n.484+27789_484+27792delinsGTCT
ENST00000410107.5:c.67+47472_67+47475delinsGTCT	ENSP00000386321.1:n.67+47472_67+47475delinsGTCT
ENST00000461400.1:n.25+26794_25+26797delinsGTCT
ENST00000474518.1:n.508+27789_508+27792delinsGTCT
ENST00000475577.5:n.254+28970_254+28973delinsGTCT
ENST00000485764.1:n.40+26794_40+26797delinsGTCT
ENST00000489225.5:n.283+63699_283+63702delinsGTCT
ENST00000489819.5:n.175+35036_175+35039delinsGTCT
ENST00000495262.5:c.925+26794_925+26797delinsGTCT	ENSP00000419411.1:n.925+26794_925+26797delinsGTCT
NM_001491.2:c.207_210delinsGTCT	NP_001482.1:p.Lys69=
NM_145649.4:c.925+26794_925+26797delinsGTCT	NP_663624.1:n.925+26794_925+26797delinsGTCT
XM_005248997.2:c.207_210delinsGTCT	XP_005249054.1:p.Lys69=
XM_005248999.2:c.694+26794_694+26797delinsGTCT	XP_005249056.1:n.694+26794_694+26797delinsGTCT
XM_006715052.2:c.925+26794_925+26797delinsGTCT	XP_006715115.1:n.925+26794_925+26797delinsGTCT
XM_011514465.1:c.926-16500_926-16497delinsGTCT	XP_011512767.1:n.926-16500_926-16497delinsGTCT
XM_011514467.1:c.694+26794_694+26797delinsGTCT	XP_011512769.1:n.694+26794_694+26797delinsGTCT
XR_926136.1:n.1476+26794_1476+26797delinsGTCT
XM_005248997.3:c.207_210delinsGTCT	XP_005249054.1:p.Lys69=
XM_006715052.3:c.925+26794_925+26797delinsGTCT	XP_006715115.1:n.925+26794_925+26797delinsGTCT
XR_002956275.1:n.1476+26794_1476+26797delinsGTCT
XR_926136.2:n.1474+26794_1474+26797delinsGTCT
NM_001374747.1:c.925+26794_925+26797delinsGTCT	NP_001361676.1:n.925+26794_925+26797delinsGTCT
NM_001491.3:c.207_210delinsGTCT MANE Plus Clinical	NP_001482.1:p.Lys69=
NM_145649.5:c.925+26794_925+26797delinsGTCT MANE Select	NP_663624.1:n.925+26794_925+26797delinsGTCT