Canonical Allele Identifier: CA380167201
Gene: EXT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44124878A>C , CM000673.2:g.44124878A>C GRCh38
NC_000011.9:g.44146428A>C , CM000673.1:g.44146428A>C GRCh37
NC_000011.8:g.44103004A>C NCBI36
NG_007560.1:g.34330A>C , LRG_494:g.34330A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.833A>C ENSP00000342656.3:p.Glu278Ala
ENST00000395673.8:c.833A>C ENSP00000379032.4:p.Glu278Ala
ENST00000531161.6:n.992A>C
ENST00000682359.1:c.833A>C ENSP00000508226.1:p.Glu278Ala
ENST00000682711.1:c.-544+29026A>C ENSP00000506803.1:n.-544+29026A>C
ENST00000682815.1:c.833A>C ENSP00000507234.1:p.Glu278Ala
ENST00000682947.1:n.1007A>C
ENST00000682993.1:c.833A>C ENSP00000507580.1:p.Glu278Ala
ENST00000683000.1:c.833A>C ENSP00000508361.1:p.Glu278Ala
ENST00000683299.1:n.1250A>C
ENST00000683870.1:c.833A>C ENSP00000507922.1:p.Glu278Ala
ENST00000683881.1:n.3394A>C
ENST00000684039.1:c.833A>C ENSP00000507677.1:p.Glu278Ala
ENST00000684124.1:c.833A>C ENSP00000508332.1:p.Glu278Ala
ENST00000684533.1:c.744-5167A>C ENSP00000507915.1:n.744-5167A>C
ENST00000533608.7:c.833A>C MANE Select ENSP00000431173.2:p.Glu278Ala
ENST00000343631.3:c.833A>C ENSP00000342656.3:p.Glu278Ala
ENST00000358681.8:c.833A>C ENSP00000351509.4:p.Glu278Ala
ENST00000395673.7:c.932A>C ENSP00000379032.3:p.Glu311Ala
ENST00000531161.5:n.10A>C
ENST00000533608.5:c.833A>C ENSP00000431173.1:p.Glu278Ala
NM_000401.3:c.932A>C , LRG_494t1:c.932A>C NP_000392.3:p.Glu311Ala
NM_001178083.1:c.833A>C NP_001171554.1:p.Glu278Ala
NM_207122.1:c.833A>C , LRG_494t2:c.833A>C NP_997005.1:p.Glu278Ala
XM_011519950.1:c.971A>C XP_011518252.1:p.Glu324Ala
XM_011519951.1:c.872A>C XP_011518253.1:p.Glu291Ala
XM_024448383.1:c.971A>C XP_024304151.1:p.Glu324Ala
NM_001178083.2:c.833A>C NP_001171554.1:p.Glu278Ala
NM_207122.2:c.833A>C MANE Select NP_997005.1:p.Glu278Ala
NM_001178083.3:c.833A>C NP_001171554.1:p.Glu278Ala
NM_001389628.1:c.833A>C NP_001376557.1:p.Glu278Ala
NM_001389630.1:c.833A>C NP_001376559.1:p.Glu278Ala