Canonical Allele Identifier: CA473811762
Gene: EXT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44148476G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44126926G>A , CM000673.2:g.44126926G>A GRCh38
NC_000011.9:g.44148476G>A , CM000673.1:g.44148476G>A GRCh37
NC_000011.8:g.44105052G>A NCBI36
NG_007560.1:g.36378G>A , LRG_494:g.36378G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.1050G>A ENSP00000342656.3:p.Leu350=
ENST00000395673.8:c.1050G>A ENSP00000379032.4:p.Leu350=
ENST00000531161.6:n.1209G>A
ENST00000682359.1:c.939+1942G>A ENSP00000508226.1:n.939+1942G>A
ENST00000682711.1:c.-544+31074G>A ENSP00000506803.1:n.-544+31074G>A
ENST00000682815.1:c.1050G>A ENSP00000507234.1:p.Leu350=
ENST00000682947.1:n.1224G>A
ENST00000682993.1:c.1050G>A ENSP00000507580.1:p.Leu350=
ENST00000683000.1:c.1050G>A ENSP00000508361.1:p.Leu350=
ENST00000683299.1:n.1467G>A
ENST00000683870.1:c.1050G>A ENSP00000507922.1:p.Leu350=
ENST00000683881.1:n.3611G>A
ENST00000684039.1:c.1050G>A ENSP00000507677.1:p.Leu350=
ENST00000684124.1:c.1050G>A ENSP00000508332.1:p.Leu350=
ENST00000684533.1:c.744-3119G>A ENSP00000507915.1:n.744-3119G>A
ENST00000533608.7:c.1050G>A MANE Select ENSP00000431173.2:p.Leu350=
ENST00000343631.3:c.1050G>A ENSP00000342656.3:p.Leu350=
ENST00000358681.8:c.1050G>A ENSP00000351509.4:p.Leu350=
ENST00000395673.7:c.1149G>A ENSP00000379032.3:p.Leu383=
ENST00000525559.1:n.24G>A
ENST00000531161.5:n.227G>A
ENST00000533608.5:c.1050G>A ENSP00000431173.1:p.Leu350=
NM_000401.3:c.1149G>A , LRG_494t1:c.1149G>A NP_000392.3:p.Leu383=
NM_001178083.1:c.1050G>A NP_001171554.1:p.Leu350=
NM_207122.1:c.1050G>A , LRG_494t2:c.1050G>A NP_997005.1:p.Leu350=
XM_011519950.1:c.1188G>A XP_011518252.1:p.Leu396=
XM_011519951.1:c.1089G>A XP_011518253.1:p.Leu363=
XM_024448383.1:c.1188G>A XP_024304151.1:p.Leu396=
NM_001178083.2:c.1050G>A NP_001171554.1:p.Leu350=
NM_207122.2:c.1050G>A MANE Select NP_997005.1:p.Leu350=
NM_001178083.3:c.1050G>A NP_001171554.1:p.Leu350=
NM_001389628.1:c.1050G>A NP_001376557.1:p.Leu350=
NM_001389630.1:c.1050G>A NP_001376559.1:p.Leu350=