Canonical Allele Identifier: CA474035368
Gene: EXT2 HGNC NCBI

Linked Data

dbSNP Id: rs2134968663
MyVariant Identifiers: chr11:g.44129766G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.44108216G>A , CM000673.2:g.44108216G>A GRCh38
NC_000011.9:g.44129766G>A , CM000673.1:g.44129766G>A GRCh37
NC_000011.8:g.44086342G>A NCBI36
NG_007560.1:g.17668G>A , LRG_494:g.17668G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000343631.4:c.504G>A ENSP00000342656.3:p.Lys168=
ENST00000395673.8:c.504G>A ENSP00000379032.4:p.Lys168=
ENST00000531161.6:n.663G>A
ENST00000682359.1:c.504G>A ENSP00000508226.1:p.Lys168=
ENST00000682711.1:c.-544+12364G>A ENSP00000506803.1:n.-544+12364G>A
ENST00000682815.1:c.504G>A ENSP00000507234.1:p.Lys168=
ENST00000682947.1:n.678G>A
ENST00000682993.1:c.504G>A ENSP00000507580.1:p.Lys168=
ENST00000683000.1:c.504G>A ENSP00000508361.1:p.Lys168=
ENST00000683299.1:n.921G>A
ENST00000683870.1:c.504G>A ENSP00000507922.1:p.Lys168=
ENST00000683881.1:n.3065G>A
ENST00000684039.1:c.504G>A ENSP00000507677.1:p.Lys168=
ENST00000684124.1:c.504G>A ENSP00000508332.1:p.Lys168=
ENST00000684533.1:c.504G>A ENSP00000507915.1:p.Lys168=
ENST00000533608.7:c.504G>A MANE Select ENSP00000431173.2:p.Lys168=
ENST00000343631.3:c.504G>A ENSP00000342656.3:p.Lys168=
ENST00000358681.8:c.504G>A ENSP00000351509.4:p.Lys168=
ENST00000395673.7:c.603G>A ENSP00000379032.3:p.Lys201=
ENST00000529186.1:n.202G>A
ENST00000533608.5:c.504G>A ENSP00000431173.1:p.Lys168=
NM_000401.3:c.603G>A , LRG_494t1:c.603G>A NP_000392.3:p.Lys201=
NM_001178083.1:c.504G>A NP_001171554.1:p.Lys168=
NM_207122.1:c.504G>A , LRG_494t2:c.504G>A NP_997005.1:p.Lys168=
XM_011519950.1:c.642G>A XP_011518252.1:p.Lys214=
XM_011519951.1:c.543G>A XP_011518253.1:p.Lys181=
XM_024448383.1:c.642G>A XP_024304151.1:p.Lys214=
NM_001178083.2:c.504G>A NP_001171554.1:p.Lys168=
NM_207122.2:c.504G>A MANE Select NP_997005.1:p.Lys168=
NM_001178083.3:c.504G>A NP_001171554.1:p.Lys168=
NM_001389628.1:c.504G>A NP_001376557.1:p.Lys168=
NM_001389630.1:c.504G>A NP_001376559.1:p.Lys168=