Canonical Allele Identifier: CA1610027463
Gene: GCNT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10555922_10555924delinsAAG , CM000668.2:g.10555922_10555924delinsAAG GRCh38
NC_000006.11:g.10556155_10556157delinsAAG , CM000668.1:g.10556155_10556157delinsAAG GRCh37
NC_000006.10:g.10664141_10664143delinsAAG NCBI36
NG_007469.3:g.68700_68702delinsAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000316170.9:c.-502_-500delinsAAG MANE Plus Clinical ENSP00000314844.3:n.-502_-500delinsAAG
ENST00000397423.7:n.484+27081_484+27083delinsAAG
ENST00000495262.7:c.925+26086_925+26088delinsAAG MANE Select ENSP00000419411.2:n.925+26086_925+26088delinsAAG
ENST00000379597.7:c.925+26086_925+26088delinsAAG ENSP00000368917.3:n.925+26086_925+26088delinsAAG
ENST00000397423.6:n.484+27081_484+27083delinsAAG
ENST00000410107.5:c.67+46764_67+46766delinsAAG ENSP00000386321.1:n.67+46764_67+46766delinsAAG
ENST00000461400.1:n.25+26086_25+26088delinsAAG
ENST00000474518.1:n.508+27081_508+27083delinsAAG
ENST00000475577.5:n.254+28262_254+28264delinsAAG
ENST00000485764.1:n.40+26086_40+26088delinsAAG
ENST00000489225.5:n.283+62991_283+62993delinsAAG
ENST00000489819.5:n.175+34328_175+34330delinsAAG
ENST00000495262.5:c.925+26086_925+26088delinsAAG ENSP00000419411.1:n.925+26086_925+26088delinsAAG
NM_001491.2:c.-502_-500delinsAAG NP_001482.1:n.-502_-500delinsAAG
NM_145649.4:c.925+26086_925+26088delinsAAG NP_663624.1:n.925+26086_925+26088delinsAAG
XM_005248999.2:c.694+26086_694+26088delinsAAG XP_005249056.1:n.694+26086_694+26088delinsAAG
XM_006715052.2:c.925+26086_925+26088delinsAAG XP_006715115.1:n.925+26086_925+26088delinsAAG
XM_006715053.2:c.1014_1016delinsAAG XP_006715116.1:p.Thr338=
XM_011514465.1:c.926-17208_926-17206delinsAAG XP_011512767.1:n.926-17208_926-17206delinsAAG
XM_011514467.1:c.694+26086_694+26088delinsAAG XP_011512769.1:n.694+26086_694+26088delinsAAG
XR_926136.1:n.1476+26086_1476+26088delinsAAG
XM_006715052.3:c.925+26086_925+26088delinsAAG XP_006715115.1:n.925+26086_925+26088delinsAAG
XR_002956275.1:n.1476+26086_1476+26088delinsAAG
XR_926136.2:n.1474+26086_1474+26088delinsAAG
NM_001374747.1:c.925+26086_925+26088delinsAAG NP_001361676.1:n.925+26086_925+26088delinsAAG
NM_001491.3:c.-502_-500delinsAAG MANE Plus Clinical NP_001482.1:n.-502_-500delinsAAG
NM_145649.5:c.925+26086_925+26088delinsAAG MANE Select NP_663624.1:n.925+26086_925+26088delinsAAG