Canonical Allele Identifier: CA380168818
Gene: EXT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44126835T>G , CM000673.2:g.44126835T>G GRCh38
NC_000011.9:g.44148385T>G , CM000673.1:g.44148385T>G GRCh37
NC_000011.8:g.44104961T>G NCBI36
NG_007560.1:g.36287T>G , LRG_494:g.36287T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.959T>G ENSP00000342656.3:p.Val320Gly
ENST00000395673.8:c.959T>G ENSP00000379032.4:p.Val320Gly
ENST00000531161.6:n.1118T>G
ENST00000682359.1:c.939+1851T>G ENSP00000508226.1:n.939+1851T>G
ENST00000682711.1:c.-544+30983T>G ENSP00000506803.1:n.-544+30983T>G
ENST00000682815.1:c.959T>G ENSP00000507234.1:p.Val320Gly
ENST00000682947.1:n.1133T>G
ENST00000682993.1:c.959T>G ENSP00000507580.1:p.Val320Gly
ENST00000683000.1:c.959T>G ENSP00000508361.1:p.Val320Gly
ENST00000683299.1:n.1376T>G
ENST00000683870.1:c.959T>G ENSP00000507922.1:p.Val320Gly
ENST00000683881.1:n.3520T>G
ENST00000684039.1:c.959T>G ENSP00000507677.1:p.Val320Gly
ENST00000684124.1:c.959T>G ENSP00000508332.1:p.Val320Gly
ENST00000684533.1:c.744-3210T>G ENSP00000507915.1:n.744-3210T>G
ENST00000533608.7:c.959T>G MANE Select ENSP00000431173.2:p.Val320Gly
ENST00000343631.3:c.959T>G ENSP00000342656.3:p.Val320Gly
ENST00000358681.8:c.959T>G ENSP00000351509.4:p.Val320Gly
ENST00000395673.7:c.1058T>G ENSP00000379032.3:p.Val353Gly
ENST00000531161.5:n.136T>G
ENST00000533608.5:c.959T>G ENSP00000431173.1:p.Val320Gly
NM_000401.3:c.1058T>G , LRG_494t1:c.1058T>G NP_000392.3:p.Val353Gly
NM_001178083.1:c.959T>G NP_001171554.1:p.Val320Gly
NM_207122.1:c.959T>G , LRG_494t2:c.959T>G NP_997005.1:p.Val320Gly
XM_011519950.1:c.1097T>G XP_011518252.1:p.Val366Gly
XM_011519951.1:c.998T>G XP_011518253.1:p.Val333Gly
XM_024448383.1:c.1097T>G XP_024304151.1:p.Val366Gly
NM_001178083.2:c.959T>G NP_001171554.1:p.Val320Gly
NM_207122.2:c.959T>G MANE Select NP_997005.1:p.Val320Gly
NM_001178083.3:c.959T>G NP_001171554.1:p.Val320Gly
NM_001389628.1:c.959T>G NP_001376557.1:p.Val320Gly
NM_001389630.1:c.959T>G NP_001376559.1:p.Val320Gly