Canonical Allele Identifier: CA5954898

Gene: EXT2

Linked Data

• dbSNP Id: rs769223470
• ExAC: 11:44129756 T / G
• gnomAD v2: 11-44129756-T-G
• gnomAD v4: 11-44108206-T-G
• MyVariant Identifiers: chr11:g.44129756T>G (hg19) ; chr11:g.44108206T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44108206T>G , CM000673.2:g.44108206T>G	GRCh38
NC_000011.9:g.44129756T>G , CM000673.1:g.44129756T>G	GRCh37
NC_000011.8:g.44086332T>G	NCBI36
NG_007560.1:g.17658T>G , LRG_494:g.17658T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.494T>G	ENSP00000342656.3:p.Leu165Arg
ENST00000395673.8:c.494T>G	ENSP00000379032.4:p.Leu165Arg
ENST00000531161.6:n.653T>G
ENST00000682359.1:c.494T>G	ENSP00000508226.1:p.Leu165Arg
ENST00000682711.1:c.-544+12354T>G	ENSP00000506803.1:n.-544+12354T>G
ENST00000682815.1:c.494T>G	ENSP00000507234.1:p.Leu165Arg
ENST00000682947.1:n.668T>G
ENST00000682993.1:c.494T>G	ENSP00000507580.1:p.Leu165Arg
ENST00000683000.1:c.494T>G	ENSP00000508361.1:p.Leu165Arg
ENST00000683299.1:n.911T>G
ENST00000683870.1:c.494T>G	ENSP00000507922.1:p.Leu165Arg
ENST00000683881.1:n.3055T>G
ENST00000684039.1:c.494T>G	ENSP00000507677.1:p.Leu165Arg
ENST00000684124.1:c.494T>G	ENSP00000508332.1:p.Leu165Arg
ENST00000684533.1:c.494T>G	ENSP00000507915.1:p.Leu165Arg
ENST00000533608.7:c.494T>G MANE Select	ENSP00000431173.2:p.Leu165Arg
ENST00000343631.3:c.494T>G	ENSP00000342656.3:p.Leu165Arg
ENST00000358681.8:c.494T>G	ENSP00000351509.4:p.Leu165Arg
ENST00000395673.7:c.593T>G	ENSP00000379032.3:p.Leu198Arg
ENST00000529186.1:n.192T>G
ENST00000533608.5:c.494T>G	ENSP00000431173.1:p.Leu165Arg
NM_000401.3:c.593T>G , LRG_494t1:c.593T>G	NP_000392.3:p.Leu198Arg
NM_001178083.1:c.494T>G	NP_001171554.1:p.Leu165Arg
NM_207122.1:c.494T>G , LRG_494t2:c.494T>G	NP_997005.1:p.Leu165Arg
XM_011519950.1:c.632T>G	XP_011518252.1:p.Leu211Arg
XM_011519951.1:c.533T>G	XP_011518253.1:p.Leu178Arg
XM_024448383.1:c.632T>G	XP_024304151.1:p.Leu211Arg
NM_001178083.2:c.494T>G	NP_001171554.1:p.Leu165Arg
NM_207122.2:c.494T>G MANE Select	NP_997005.1:p.Leu165Arg
NM_001178083.3:c.494T>G	NP_001171554.1:p.Leu165Arg
NM_001389628.1:c.494T>G	NP_001376557.1:p.Leu165Arg
NM_001389630.1:c.494T>G	NP_001376559.1:p.Leu165Arg