Canonical Allele Identifier: CA473811775
Gene: EXT2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.44148488A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44126938A>G , CM000673.2:g.44126938A>G GRCh38
NC_000011.9:g.44148488A>G , CM000673.1:g.44148488A>G GRCh37
NC_000011.8:g.44105064A>G NCBI36
NG_007560.1:g.36390A>G , LRG_494:g.36390A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.1062A>G ENSP00000342656.3:p.Glu354=
ENST00000395673.8:c.1062A>G ENSP00000379032.4:p.Glu354=
ENST00000531161.6:n.1221A>G
ENST00000682359.1:c.939+1954A>G ENSP00000508226.1:n.939+1954A>G
ENST00000682711.1:c.-544+31086A>G ENSP00000506803.1:n.-544+31086A>G
ENST00000682815.1:c.1062A>G ENSP00000507234.1:p.Glu354=
ENST00000682947.1:n.1236A>G
ENST00000682993.1:c.1062A>G ENSP00000507580.1:p.Glu354=
ENST00000683000.1:c.1062A>G ENSP00000508361.1:p.Glu354=
ENST00000683299.1:n.1479A>G
ENST00000683870.1:c.1062A>G ENSP00000507922.1:p.Glu354=
ENST00000683881.1:n.3623A>G
ENST00000684039.1:c.1062A>G ENSP00000507677.1:p.Glu354=
ENST00000684124.1:c.1062A>G ENSP00000508332.1:p.Glu354=
ENST00000684533.1:c.744-3107A>G ENSP00000507915.1:n.744-3107A>G
ENST00000533608.7:c.1062A>G MANE Select ENSP00000431173.2:p.Glu354=
ENST00000343631.3:c.1062A>G ENSP00000342656.3:p.Glu354=
ENST00000358681.8:c.1062A>G ENSP00000351509.4:p.Glu354=
ENST00000395673.7:c.1161A>G ENSP00000379032.3:p.Glu387=
ENST00000525559.1:n.36A>G
ENST00000531161.5:n.239A>G
ENST00000533608.5:c.1062A>G ENSP00000431173.1:p.Glu354=
NM_000401.3:c.1161A>G , LRG_494t1:c.1161A>G NP_000392.3:p.Glu387=
NM_001178083.1:c.1062A>G NP_001171554.1:p.Glu354=
NM_207122.1:c.1062A>G , LRG_494t2:c.1062A>G NP_997005.1:p.Glu354=
XM_011519950.1:c.1200A>G XP_011518252.1:p.Glu400=
XM_011519951.1:c.1101A>G XP_011518253.1:p.Glu367=
XM_024448383.1:c.1200A>G XP_024304151.1:p.Glu400=
NM_001178083.2:c.1062A>G NP_001171554.1:p.Glu354=
NM_207122.2:c.1062A>G MANE Select NP_997005.1:p.Glu354=
NM_001178083.3:c.1062A>G NP_001171554.1:p.Glu354=
NM_001389628.1:c.1062A>G NP_001376557.1:p.Glu354=
NM_001389630.1:c.1062A>G NP_001376559.1:p.Glu354=