Canonical Allele Identifier: CA380169156

Gene: EXT2

Linked Data

• gnomAD v4: 11-44126913-A-T
• MyVariant Identifiers: chr11:g.44148463A>T (hg19) ; chr11:g.44126913A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.44126913A>T , CM000673.2:g.44126913A>T	GRCh38
NC_000011.9:g.44148463A>T , CM000673.1:g.44148463A>T	GRCh37
NC_000011.8:g.44105039A>T	NCBI36
NG_007560.1:g.36365A>T , LRG_494:g.36365A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000343631.4:c.1037A>T	ENSP00000342656.3:p.Asp346Val
ENST00000395673.8:c.1037A>T	ENSP00000379032.4:p.Asp346Val
ENST00000531161.6:n.1196A>T
ENST00000682359.1:c.939+1929A>T	ENSP00000508226.1:n.939+1929A>T
ENST00000682711.1:c.-544+31061A>T	ENSP00000506803.1:n.-544+31061A>T
ENST00000682815.1:c.1037A>T	ENSP00000507234.1:p.Asp346Val
ENST00000682947.1:n.1211A>T
ENST00000682993.1:c.1037A>T	ENSP00000507580.1:p.Asp346Val
ENST00000683000.1:c.1037A>T	ENSP00000508361.1:p.Asp346Val
ENST00000683299.1:n.1454A>T
ENST00000683870.1:c.1037A>T	ENSP00000507922.1:p.Asp346Val
ENST00000683881.1:n.3598A>T
ENST00000684039.1:c.1037A>T	ENSP00000507677.1:p.Asp346Val
ENST00000684124.1:c.1037A>T	ENSP00000508332.1:p.Asp346Val
ENST00000684533.1:c.744-3132A>T	ENSP00000507915.1:n.744-3132A>T
ENST00000533608.7:c.1037A>T MANE Select	ENSP00000431173.2:p.Asp346Val
ENST00000343631.3:c.1037A>T	ENSP00000342656.3:p.Asp346Val
ENST00000358681.8:c.1037A>T	ENSP00000351509.4:p.Asp346Val
ENST00000395673.7:c.1136A>T	ENSP00000379032.3:p.Asp379Val
ENST00000525559.1:n.11A>T
ENST00000531161.5:n.214A>T
ENST00000533608.5:c.1037A>T	ENSP00000431173.1:p.Asp346Val
NM_000401.3:c.1136A>T , LRG_494t1:c.1136A>T	NP_000392.3:p.Asp379Val
NM_001178083.1:c.1037A>T	NP_001171554.1:p.Asp346Val
NM_207122.1:c.1037A>T , LRG_494t2:c.1037A>T	NP_997005.1:p.Asp346Val
XM_011519950.1:c.1175A>T	XP_011518252.1:p.Asp392Val
XM_011519951.1:c.1076A>T	XP_011518253.1:p.Asp359Val
XM_024448383.1:c.1175A>T	XP_024304151.1:p.Asp392Val
NM_001178083.2:c.1037A>T	NP_001171554.1:p.Asp346Val
NM_207122.2:c.1037A>T MANE Select	NP_997005.1:p.Asp346Val
NM_001178083.3:c.1037A>T	NP_001171554.1:p.Asp346Val
NM_001389628.1:c.1037A>T	NP_001376557.1:p.Asp346Val
NM_001389630.1:c.1037A>T	NP_001376559.1:p.Asp346Val