Canonical Allele Identifier: CA2695213773
Gene: EXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44107956_44107957insC , CM000673.2:g.44107956_44107957insC GRCh38
NC_000011.9:g.44129506_44129507insC , CM000673.1:g.44129506_44129507insC GRCh37
NC_000011.8:g.44086082_44086083insC NCBI36
NG_007560.1:g.17408_17409insC , LRG_494:g.17408_17409insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.244_245insC ENSP00000342656.3:p.Asp82AlafsTer11
ENST00000395673.8:c.244_245insC ENSP00000379032.4:p.Asp82AlafsTer11
ENST00000531161.6:n.403_404insC
ENST00000682359.1:c.244_245insC ENSP00000508226.1:p.Asp82AlafsTer11
ENST00000682711.1:c.-544+12104_-544+12105insC ENSP00000506803.1:n.-544+12104_-544+12105insC
ENST00000682815.1:c.244_245insC ENSP00000507234.1:p.Asp82AlafsTer11
ENST00000682947.1:n.418_419insC
ENST00000682993.1:c.244_245insC ENSP00000507580.1:p.Asp82AlafsTer11
ENST00000683000.1:c.244_245insC ENSP00000508361.1:p.Asp82AlafsTer11
ENST00000683299.1:n.661_662insC
ENST00000683870.1:c.244_245insC ENSP00000507922.1:p.Asp82AlafsTer11
ENST00000683881.1:n.2805_2806insC
ENST00000684039.1:c.244_245insC ENSP00000507677.1:p.Asp82AlafsTer11
ENST00000684124.1:c.244_245insC ENSP00000508332.1:p.Asp82AlafsTer11
ENST00000684533.1:c.244_245insC ENSP00000507915.1:p.Asp82AlafsTer11
ENST00000533608.7:c.244_245insC MANE Select ENSP00000431173.2:p.Asp82AlafsTer11
ENST00000343631.3:c.244_245insC ENSP00000342656.3:p.Asp82AlafsTer11
ENST00000358681.8:c.244_245insC ENSP00000351509.4:p.Asp82AlafsTer11
ENST00000395673.7:c.343_344insC ENSP00000379032.3:p.Asp115AlafsTer11
ENST00000527014.1:c.244_245insC ENSP00000434716.1:p.Asp82AlafsTer11
ENST00000533608.5:c.244_245insC ENSP00000431173.1:p.Asp82AlafsTer11
NM_000401.3:c.343_344insC , LRG_494t1:c.343_344insC NP_000392.3:p.Asp115AlafsTer11
NM_001178083.1:c.244_245insC NP_001171554.1:p.Asp82AlafsTer11
NM_207122.1:c.244_245insC , LRG_494t2:c.244_245insC NP_997005.1:p.Asp82AlafsTer11
XM_011519950.1:c.382_383insC XP_011518252.1:p.Asp128AlafsTer11
XM_011519951.1:c.283_284insC XP_011518253.1:p.Asp95AlafsTer11
XM_024448383.1:c.382_383insC XP_024304151.1:p.Asp128AlafsTer11
NM_001178083.2:c.244_245insC NP_001171554.1:p.Asp82AlafsTer11
NM_207122.2:c.244_245insC MANE Select NP_997005.1:p.Asp82AlafsTer11
NM_001178083.3:c.244_245insC NP_001171554.1:p.Asp82AlafsTer11
NM_001389628.1:c.244_245insC NP_001376557.1:p.Asp82AlafsTer11
NM_001389630.1:c.244_245insC NP_001376559.1:p.Asp82AlafsTer11