Canonical Allele Identifier: CA1967882619
Gene: EXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44124824_44124826delinsGTC , CM000673.2:g.44124824_44124826delinsGTC GRCh38
NC_000011.9:g.44146374_44146376delinsGTC , CM000673.1:g.44146374_44146376delinsGTC GRCh37
NC_000011.8:g.44102950_44102952delinsGTC NCBI36
NG_007560.1:g.34276_34278delinsGTC , LRG_494:g.34276_34278delinsGTC

Transcript Alleles

HGVS Amino-acid change
ENST00000343631.4:c.779_781delinsGTC ENSP00000342656.3:p.Gly260=
ENST00000395673.8:c.779_781delinsGTC ENSP00000379032.4:p.Gly260=
ENST00000531161.6:n.938_940delinsGTC
ENST00000682359.1:c.779_781delinsGTC ENSP00000508226.1:p.Gly260=
ENST00000682711.1:c.-544+28972_-544+28974delinsGTC ENSP00000506803.1:n.-544+28972_-544+28974...
ENST00000682815.1:c.779_781delinsGTC ENSP00000507234.1:p.Gly260=
ENST00000682947.1:n.953_955delinsGTC
ENST00000682993.1:c.779_781delinsGTC ENSP00000507580.1:p.Gly260=
ENST00000683000.1:c.779_781delinsGTC ENSP00000508361.1:p.Gly260=
ENST00000683299.1:n.1196_1198delinsGTC
ENST00000683870.1:c.779_781delinsGTC ENSP00000507922.1:p.Gly260=
ENST00000683881.1:n.3340_3342delinsGTC
ENST00000684039.1:c.779_781delinsGTC ENSP00000507677.1:p.Gly260=
ENST00000684124.1:c.779_781delinsGTC ENSP00000508332.1:p.Gly260=
ENST00000684533.1:c.744-5221_744-5219delinsGTC ENSP00000507915.1:n.744-5221_744-5219deli...
ENST00000533608.7:c.779_781delinsGTC MANE Select ENSP00000431173.2:p.Gly260=
ENST00000343631.3:c.779_781delinsGTC ENSP00000342656.3:p.Gly260=
ENST00000358681.8:c.779_781delinsGTC ENSP00000351509.4:p.Gly260=
ENST00000395673.7:c.878_880delinsGTC ENSP00000379032.3:p.Gly293=
ENST00000533608.5:c.779_781delinsGTC ENSP00000431173.1:p.Gly260=
NM_000401.3:c.878_880delinsGTC , LRG_494t1:c.878_880delinsGTC NP_000392.3:p.Gly293=
NM_001178083.1:c.779_781delinsGTC NP_001171554.1:p.Gly260=
NM_207122.1:c.779_781delinsGTC , LRG_494t2:c.779_781delinsGTC NP_997005.1:p.Gly260=
XM_011519950.1:c.917_919delinsGTC XP_011518252.1:p.Gly306=
XM_011519951.1:c.818_820delinsGTC XP_011518253.1:p.Gly273=
XM_024448383.1:c.917_919delinsGTC XP_024304151.1:p.Gly306=
NM_001178083.2:c.779_781delinsGTC NP_001171554.1:p.Gly260=
NM_207122.2:c.779_781delinsGTC MANE Select NP_997005.1:p.Gly260=
NM_001178083.3:c.779_781delinsGTC NP_001171554.1:p.Gly260=
NM_001389628.1:c.779_781delinsGTC NP_001376557.1:p.Gly260=
NM_001389630.1:c.779_781delinsGTC NP_001376559.1:p.Gly260=