Canonical Allele Identifier: CA1967883535
Gene: EXT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44126949G= , CM000673.2:g.44126949G= GRCh38
NC_000011.9:g.44148499G= , CM000673.1:g.44148499G= GRCh37
NC_000011.8:g.44105075G= NCBI36
NG_007560.1:g.36401G= , LRG_494:g.36401G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.1073G= ENSP00000342656.3:p.Trp358=
ENST00000395673.8:c.1073G= ENSP00000379032.4:p.Trp358=
ENST00000531161.6:n.1232G=
ENST00000682359.1:c.939+1965G= ENSP00000508226.1:n.939+1965G=
ENST00000682711.1:c.-544+31097G= ENSP00000506803.1:n.-544+31097G=
ENST00000682815.1:c.1073G= ENSP00000507234.1:p.Trp358=
ENST00000682947.1:n.1247G=
ENST00000682993.1:c.1073G= ENSP00000507580.1:p.Trp358=
ENST00000683000.1:c.1073G= ENSP00000508361.1:p.Trp358=
ENST00000683299.1:n.1490G=
ENST00000683870.1:c.1073G= ENSP00000507922.1:p.Trp358=
ENST00000683881.1:n.3634G=
ENST00000684039.1:c.1073G= ENSP00000507677.1:p.Trp358=
ENST00000684124.1:c.1073G= ENSP00000508332.1:p.Trp358=
ENST00000684533.1:c.744-3096G= ENSP00000507915.1:n.744-3096G=
ENST00000533608.7:c.1073G= MANE Select ENSP00000431173.2:p.Trp358=
ENST00000343631.3:c.1073G= ENSP00000342656.3:p.Trp358=
ENST00000358681.8:c.1073G= ENSP00000351509.4:p.Trp358=
ENST00000395673.7:c.1172G= ENSP00000379032.3:p.Trp391=
ENST00000525559.1:n.47G=
ENST00000531161.5:n.250G=
ENST00000533608.5:c.1073G= ENSP00000431173.1:p.Trp358=
NM_000401.3:c.1172G= , LRG_494t1:c.1172G= NP_000392.3:p.Trp391=
NM_001178083.1:c.1073G= NP_001171554.1:p.Trp358=
NM_207122.1:c.1073G= , LRG_494t2:c.1073G= NP_997005.1:p.Trp358=
XM_011519950.1:c.1211G= XP_011518252.1:p.Trp404=
XM_011519951.1:c.1112G= XP_011518253.1:p.Trp371=
XM_024448383.1:c.1211G= XP_024304151.1:p.Trp404=
NM_001178083.2:c.1073G= NP_001171554.1:p.Trp358=
NM_207122.2:c.1073G= MANE Select NP_997005.1:p.Trp358=
NM_001178083.3:c.1073G= NP_001171554.1:p.Trp358=
NM_001389628.1:c.1073G= NP_001376557.1:p.Trp358=
NM_001389630.1:c.1073G= NP_001376559.1:p.Trp358=