Canonical Allele Identifier: CA2677293146
Gene: GCNT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10529867_10529868insTAAA , CM000668.2:g.10529867_10529868insTAAA GRCh38
NC_000006.11:g.10530100_10530101insTAAA , CM000668.1:g.10530100_10530101insTAAA GRCh37
NC_000006.10:g.10638086_10638087insTAAA NCBI36
NG_007469.3:g.42645_42646insTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000397423.7:n.484+1026_484+1027insTAAA
ENST00000495262.7:c.925+31_925+32insTAAA MANE Select ENSP00000419411.2:n.925+31_925+32insTAAA
ENST00000379597.7:c.925+31_925+32insTAAA ENSP00000368917.3:n.925+31_925+32insTAAA
ENST00000397423.6:n.484+1026_484+1027insTAAA
ENST00000410107.5:c.67+20709_67+20710insTAAA ENSP00000386321.1:n.67+20709_67+20710insTAAA
ENST00000461400.1:n.25+31_25+32insTAAA
ENST00000474518.1:n.508+1026_508+1027insTAAA
ENST00000474983.5:n.1533_1534insTAAA
ENST00000475577.5:n.254+2207_254+2208insTAAA
ENST00000483204.1:n.1532_1533insTAAA
ENST00000485764.1:n.40+31_40+32insTAAA
ENST00000489225.5:n.283+36936_283+36937insTAAA
ENST00000489819.5:n.175+8273_175+8274insTAAA
ENST00000495262.5:c.925+31_925+32insTAAA ENSP00000419411.1:n.925+31_925+32insTAAA
NM_145649.4:c.925+31_925+32insTAAA NP_663624.1:n.925+31_925+32insTAAA
XM_005248999.2:c.694+31_694+32insTAAA XP_005249056.1:n.694+31_694+32insTAAA
XM_006715052.2:c.925+31_925+32insTAAA XP_006715115.1:n.925+31_925+32insTAAA
XM_006715053.2:c.925+31_925+32insTAAA XP_006715116.1:n.925+31_925+32insTAAA
XM_011514465.1:c.925+31_925+32insTAAA XP_011512767.1:n.925+31_925+32insTAAA
XM_011514467.1:c.694+31_694+32insTAAA XP_011512769.1:n.694+31_694+32insTAAA
XM_011514468.1:c.925+31_925+32insTAAA XP_011512770.1:n.925+31_925+32insTAAA
XR_926136.1:n.1476+31_1476+32insTAAA
XM_006715052.3:c.925+31_925+32insTAAA XP_006715115.1:n.925+31_925+32insTAAA
XM_011514468.3:c.925+31_925+32insTAAA XP_011512770.1:n.925+31_925+32insTAAA
XM_017010732.2:c.925+31_925+32insTAAA XP_016866221.1:n.925+31_925+32insTAAA
XR_002956275.1:n.1476+31_1476+32insTAAA
XR_926136.2:n.1474+31_1474+32insTAAA
NM_001374747.1:c.925+31_925+32insTAAA NP_001361676.1:n.925+31_925+32insTAAA
NM_145649.5:c.925+31_925+32insTAAA MANE Select NP_663624.1:n.925+31_925+32insTAAA