Canonical Allele Identifier: CA1610028562

Gene: GCNT2

Linked Data

• dbSNP Id: rs1762718689

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10556630_10556631insACGATAAAAATAA , CM000668.2:g.10556630_10556631insACGATAAAAATAA	GRCh38
NC_000006.11:g.10556863_10556864insACGATAAAAATAA , CM000668.1:g.10556863_10556864insACGATAAAAATAA	GRCh37
NC_000006.10:g.10664849_10664850insACGATAAAAATAA	NCBI36
NG_007469.3:g.69408_69409insACGATAAAAATAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316170.9:c.207_208insACGATAAAAATAA MANE Plus Clinical	ENSP00000314844.3:p.Ser70ThrfsTer23
ENST00000397423.7:n.484+27789_484+27790insACGATAAAAATAA
ENST00000495262.7:c.925+26794_925+26795insACGATAAAAATAA MANE Select	ENSP00000419411.2:n.925+26794_925+26795insACGATAAAAATAA
ENST00000640968.1:c.207_208insACGATAAAAATAA	ENSP00000492466.1:p.Ser70ThrfsTer23
ENST00000316170.7:c.207_208insACGATAAAAATAA	ENSP00000314844.3:p.Ser70ThrfsTer23
ENST00000379597.7:c.925+26794_925+26795insACGATAAAAATAA	ENSP00000368917.3:n.925+26794_925+26795insACGATAAAAATAA
ENST00000397423.6:n.484+27789_484+27790insACGATAAAAATAA
ENST00000410107.5:c.67+47472_67+47473insACGATAAAAATAA	ENSP00000386321.1:n.67+47472_67+47473insACGATAAAAATAA
ENST00000461400.1:n.25+26794_25+26795insACGATAAAAATAA
ENST00000474518.1:n.508+27789_508+27790insACGATAAAAATAA
ENST00000475577.5:n.254+28970_254+28971insACGATAAAAATAA
ENST00000485764.1:n.40+26794_40+26795insACGATAAAAATAA
ENST00000489225.5:n.283+63699_283+63700insACGATAAAAATAA
ENST00000489819.5:n.175+35036_175+35037insACGATAAAAATAA
ENST00000495262.5:c.925+26794_925+26795insACGATAAAAATAA	ENSP00000419411.1:n.925+26794_925+26795insACGATAAAAATAA
NM_001491.2:c.207_208insACGATAAAAATAA	NP_001482.1:p.Ser70ThrfsTer23
NM_145649.4:c.925+26794_925+26795insACGATAAAAATAA	NP_663624.1:n.925+26794_925+26795insACGATAAAAATAA
XM_005248997.2:c.207_208insACGATAAAAATAA	XP_005249054.1:p.Ser70ThrfsTer23
XM_005248999.2:c.694+26794_694+26795insACGATAAAAATAA	XP_005249056.1:n.694+26794_694+26795insACGATAAAAATAA
XM_006715052.2:c.925+26794_925+26795insACGATAAAAATAA	XP_006715115.1:n.925+26794_925+26795insACGATAAAAATAA
XM_011514465.1:c.926-16500_926-16499insACGATAAAAATAA	XP_011512767.1:n.926-16500_926-16499insACGATAAAAATAA
XM_011514467.1:c.694+26794_694+26795insACGATAAAAATAA	XP_011512769.1:n.694+26794_694+26795insACGATAAAAATAA
XR_926136.1:n.1476+26794_1476+26795insACGATAAAAATAA
XM_005248997.3:c.207_208insACGATAAAAATAA	XP_005249054.1:p.Ser70ThrfsTer23
XM_006715052.3:c.925+26794_925+26795insACGATAAAAATAA	XP_006715115.1:n.925+26794_925+26795insACGATAAAAATAA
XR_002956275.1:n.1476+26794_1476+26795insACGATAAAAATAA
XR_926136.2:n.1474+26794_1474+26795insACGATAAAAATAA
NM_001374747.1:c.925+26794_925+26795insACGATAAAAATAA	NP_001361676.1:n.925+26794_925+26795insACGATAAAAATAA
NM_001491.3:c.207_208insACGATAAAAATAA MANE Plus Clinical	NP_001482.1:p.Ser70ThrfsTer23
NM_145649.5:c.925+26794_925+26795insACGATAAAAATAA MANE Select	NP_663624.1:n.925+26794_925+26795insACGATAAAAATAA