Canonical Allele Identifier: CA380179375
Gene: EXT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44107699C>A , CM000673.2:g.44107699C>A GRCh38
NC_000011.9:g.44129249C>A , CM000673.1:g.44129249C>A GRCh37
NC_000011.8:g.44085825C>A NCBI36
NG_007560.1:g.17151C>A , LRG_494:g.17151C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.-14C>A ENSP00000342656.3:n.-14C>A
ENST00000395673.8:c.-14C>A ENSP00000379032.4:n.-14C>A
ENST00000531161.6:n.146C>A
ENST00000682359.1:c.-14C>A ENSP00000508226.1:n.-14C>A
ENST00000682711.1:c.-544+11847C>A ENSP00000506803.1:n.-544+11847C>A
ENST00000682815.1:c.-14C>A ENSP00000507234.1:n.-14C>A
ENST00000682947.1:n.161C>A
ENST00000682993.1:c.-14C>A ENSP00000507580.1:n.-14C>A
ENST00000683000.1:c.-14C>A ENSP00000508361.1:n.-14C>A
ENST00000683299.1:n.404C>A
ENST00000683870.1:c.-14C>A ENSP00000507922.1:n.-14C>A
ENST00000683881.1:n.2548C>A
ENST00000684039.1:c.-14C>A ENSP00000507677.1:n.-14C>A
ENST00000684124.1:c.-14C>A ENSP00000508332.1:n.-14C>A
ENST00000684533.1:c.-14C>A ENSP00000507915.1:n.-14C>A
ENST00000533608.7:c.-14C>A MANE Select ENSP00000431173.2:n.-14C>A
ENST00000343631.3:c.-14C>A ENSP00000342656.3:n.-14C>A
ENST00000358681.8:c.-14C>A ENSP00000351509.4:n.-14C>A
ENST00000395673.7:c.86C>A ENSP00000379032.3:p.Ala29Asp
ENST00000527014.1:c.-14C>A ENSP00000434716.1:n.-14C>A
ENST00000532479.1:c.-14C>A ENSP00000433827.1:n.-14C>A
ENST00000533608.5:c.-14C>A ENSP00000431173.1:n.-14C>A
NM_000401.3:c.86C>A , LRG_494t1:c.86C>A NP_000392.3:p.Ala29Asp
NM_001178083.1:c.-14C>A NP_001171554.1:n.-14C>A
NM_207122.1:c.-14C>A , LRG_494t2:c.-14C>A NP_997005.1:n.-14C>A
XM_011519950.1:c.125C>A XP_011518252.1:p.Ala42Asp
XM_011519951.1:c.26C>A XP_011518253.1:p.Ala9Asp
XM_024448383.1:c.125C>A XP_024304151.1:p.Ala42Asp
NM_001178083.2:c.-14C>A NP_001171554.1:n.-14C>A
NM_207122.2:c.-14C>A MANE Select NP_997005.1:n.-14C>A
NM_001178083.3:c.-14C>A NP_001171554.1:n.-14C>A
NM_001389628.1:c.-14C>A NP_001376557.1:n.-14C>A
NM_001389630.1:c.-14C>A NP_001376559.1:n.-14C>A