Canonical Allele Identifier: CA1610028747

Gene: GCNT2

Linked Data

• dbSNP Id: rs1762727369

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556753_10556754insA , CM000668.2:g.10556753_10556754insA	GRCh38
NC_000006.11:g.10556986_10556987insA , CM000668.1:g.10556986_10556987insA	GRCh37
NC_000006.10:g.10664972_10664973insA	NCBI36
NG_007469.3:g.69531_69532insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.330_331insA MANE Plus Clinical	ENSP00000314844.3:p.Leu111ThrfsTer18
ENST00000397423.7:n.484+27912_484+27913insA
ENST00000495262.7:c.925+26917_925+26918insA MANE Select	ENSP00000419411.2:n.925+26917_925+26918insA
ENST00000640968.1:c.330_331insA	ENSP00000492466.1:p.Leu111ThrfsTer18
ENST00000316170.7:c.330_331insA	ENSP00000314844.3:p.Leu111ThrfsTer18
ENST00000379597.7:c.925+26917_925+26918insA	ENSP00000368917.3:n.925+26917_925+26918insA
ENST00000397423.6:n.484+27912_484+27913insA
ENST00000410107.5:c.67+47595_67+47596insA	ENSP00000386321.1:n.67+47595_67+47596insA
ENST00000461400.1:n.25+26917_25+26918insA
ENST00000474518.1:n.508+27912_508+27913insA
ENST00000475577.5:n.254+29093_254+29094insA
ENST00000485764.1:n.40+26917_40+26918insA
ENST00000489225.5:n.283+63822_283+63823insA
ENST00000489819.5:n.175+35159_175+35160insA
ENST00000495262.5:c.925+26917_925+26918insA	ENSP00000419411.1:n.925+26917_925+26918insA
NM_001491.2:c.330_331insA	NP_001482.1:p.Leu111ThrfsTer18
NM_145649.4:c.925+26917_925+26918insA	NP_663624.1:n.925+26917_925+26918insA
XM_005248997.2:c.330_331insA	XP_005249054.1:p.Leu111ThrfsTer18
XM_005248999.2:c.694+26917_694+26918insA	XP_005249056.1:n.694+26917_694+26918insA
XM_006715052.2:c.925+26917_925+26918insA	XP_006715115.1:n.925+26917_925+26918insA
XM_011514465.1:c.926-16377_926-16376insA	XP_011512767.1:n.926-16377_926-16376insA
XM_011514467.1:c.694+26917_694+26918insA	XP_011512769.1:n.694+26917_694+26918insA
XR_926136.1:n.1476+26917_1476+26918insA
XM_005248997.3:c.330_331insA	XP_005249054.1:p.Leu111ThrfsTer18
XM_006715052.3:c.925+26917_925+26918insA	XP_006715115.1:n.925+26917_925+26918insA
XR_002956275.1:n.1476+26917_1476+26918insA
XR_926136.2:n.1474+26917_1474+26918insA
NM_001374747.1:c.925+26917_925+26918insA	NP_001361676.1:n.925+26917_925+26918insA
NM_001491.3:c.330_331insA MANE Plus Clinical	NP_001482.1:p.Leu111ThrfsTer18
NM_145649.5:c.925+26917_925+26918insA MANE Select	NP_663624.1:n.925+26917_925+26918insA