Canonical Allele Identifier: CA1967875015
Gene: EXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44107698_44107699delinsGC , CM000673.2:g.44107698_44107699delinsGC GRCh38
NC_000011.9:g.44129248_44129249delinsGC , CM000673.1:g.44129248_44129249delinsGC GRCh37
NC_000011.8:g.44085824_44085825delinsGC NCBI36
NG_007560.1:g.17150_17151delinsGC , LRG_494:g.17150_17151delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.-15_-14delinsGC ENSP00000342656.3:n.-15_-14delinsGC
ENST00000395673.8:c.-15_-14delinsGC ENSP00000379032.4:n.-15_-14delinsGC
ENST00000531161.6:n.145_146delinsGC
ENST00000682359.1:c.-15_-14delinsGC ENSP00000508226.1:n.-15_-14delinsGC
ENST00000682711.1:c.-544+11846_-544+11847delinsGC ENSP00000506803.1:n.-544+11846_-544+11847delinsGC
ENST00000682815.1:c.-15_-14delinsGC ENSP00000507234.1:n.-15_-14delinsGC
ENST00000682947.1:n.160_161delinsGC
ENST00000682993.1:c.-15_-14delinsGC ENSP00000507580.1:n.-15_-14delinsGC
ENST00000683000.1:c.-15_-14delinsGC ENSP00000508361.1:n.-15_-14delinsGC
ENST00000683299.1:n.403_404delinsGC
ENST00000683870.1:c.-15_-14delinsGC ENSP00000507922.1:n.-15_-14delinsGC
ENST00000683881.1:n.2547_2548delinsGC
ENST00000684039.1:c.-15_-14delinsGC ENSP00000507677.1:n.-15_-14delinsGC
ENST00000684124.1:c.-15_-14delinsGC ENSP00000508332.1:n.-15_-14delinsGC
ENST00000684533.1:c.-15_-14delinsGC ENSP00000507915.1:n.-15_-14delinsGC
ENST00000533608.7:c.-15_-14delinsGC MANE Select ENSP00000431173.2:n.-15_-14delinsGC
ENST00000343631.3:c.-15_-14delinsGC ENSP00000342656.3:n.-15_-14delinsGC
ENST00000358681.8:c.-15_-14delinsGC ENSP00000351509.4:n.-15_-14delinsGC
ENST00000395673.7:c.85_86delinsGC ENSP00000379032.3:p.Ala29=
ENST00000527014.1:c.-15_-14delinsGC ENSP00000434716.1:n.-15_-14delinsGC
ENST00000532479.1:c.-15_-14delinsGC ENSP00000433827.1:n.-15_-14delinsGC
ENST00000533608.5:c.-15_-14delinsGC ENSP00000431173.1:n.-15_-14delinsGC
NM_000401.3:c.85_86delinsGC , LRG_494t1:c.85_86delinsGC NP_000392.3:p.Ala29=
NM_001178083.1:c.-15_-14delinsGC NP_001171554.1:n.-15_-14delinsGC
NM_207122.1:c.-15_-14delinsGC , LRG_494t2:c.-15_-14delinsGC NP_997005.1:n.-15_-14delinsGC
XM_011519950.1:c.124_125delinsGC XP_011518252.1:p.Ala42=
XM_011519951.1:c.25_26delinsGC XP_011518253.1:p.Ala9=
XM_024448383.1:c.124_125delinsGC XP_024304151.1:p.Ala42=
NM_001178083.2:c.-15_-14delinsGC NP_001171554.1:n.-15_-14delinsGC
NM_207122.2:c.-15_-14delinsGC MANE Select NP_997005.1:n.-15_-14delinsGC
NM_001178083.3:c.-15_-14delinsGC NP_001171554.1:n.-15_-14delinsGC
NM_001389628.1:c.-15_-14delinsGC NP_001376557.1:n.-15_-14delinsGC
NM_001389630.1:c.-15_-14delinsGC NP_001376559.1:n.-15_-14delinsGC