Canonical Allele Identifier: CA1967875102
Gene: EXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44107735_44107736delinsAT , CM000673.2:g.44107735_44107736delinsAT GRCh38
NC_000011.9:g.44129285_44129286delinsAT , CM000673.1:g.44129285_44129286delinsAT GRCh37
NC_000011.8:g.44085861_44085862delinsAT NCBI36
NG_007560.1:g.17187_17188delinsAT , LRG_494:g.17187_17188delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000343631.4:c.23_24delinsAT ENSP00000342656.3:p.Asn8=
ENST00000395673.8:c.23_24delinsAT ENSP00000379032.4:p.Asn8=
ENST00000531161.6:n.182_183delinsAT
ENST00000682359.1:c.23_24delinsAT ENSP00000508226.1:p.Asn8=
ENST00000682711.1:c.-544+11883_-544+11884delinsAT ENSP00000506803.1:n.-544+11883_-544+11884...
ENST00000682815.1:c.23_24delinsAT ENSP00000507234.1:p.Asn8=
ENST00000682947.1:n.197_198delinsAT
ENST00000682993.1:c.23_24delinsAT ENSP00000507580.1:p.Asn8=
ENST00000683000.1:c.23_24delinsAT ENSP00000508361.1:p.Asn8=
ENST00000683299.1:n.440_441delinsAT
ENST00000683870.1:c.23_24delinsAT ENSP00000507922.1:p.Asn8=
ENST00000683881.1:n.2584_2585delinsAT
ENST00000684039.1:c.23_24delinsAT ENSP00000507677.1:p.Asn8=
ENST00000684124.1:c.23_24delinsAT ENSP00000508332.1:p.Asn8=
ENST00000684533.1:c.23_24delinsAT ENSP00000507915.1:p.Asn8=
ENST00000533608.7:c.23_24delinsAT MANE Select ENSP00000431173.2:p.Asn8=
ENST00000343631.3:c.23_24delinsAT ENSP00000342656.3:p.Asn8=
ENST00000358681.8:c.23_24delinsAT ENSP00000351509.4:p.Asn8=
ENST00000395673.7:c.122_123delinsAT ENSP00000379032.3:p.Asn41=
ENST00000527014.1:c.23_24delinsAT ENSP00000434716.1:p.Asn8=
ENST00000532479.1:c.23_24delinsAT ENSP00000433827.1:p.Asn8=
ENST00000533608.5:c.23_24delinsAT ENSP00000431173.1:p.Asn8=
NM_000401.3:c.122_123delinsAT , LRG_494t1:c.122_123delinsAT NP_000392.3:p.Asn41=
NM_001178083.1:c.23_24delinsAT NP_001171554.1:p.Asn8=
NM_207122.1:c.23_24delinsAT , LRG_494t2:c.23_24delinsAT NP_997005.1:p.Asn8=
XM_011519950.1:c.161_162delinsAT XP_011518252.1:p.Asn54=
XM_011519951.1:c.62_63delinsAT XP_011518253.1:p.Asn21=
XM_024448383.1:c.161_162delinsAT XP_024304151.1:p.Asn54=
NM_001178083.2:c.23_24delinsAT NP_001171554.1:p.Asn8=
NM_207122.2:c.23_24delinsAT MANE Select NP_997005.1:p.Asn8=
NM_001178083.3:c.23_24delinsAT NP_001171554.1:p.Asn8=
NM_001389628.1:c.23_24delinsAT NP_001376557.1:p.Asn8=
NM_001389630.1:c.23_24delinsAT NP_001376559.1:p.Asn8=