Canonical Allele Identifier: CA350690264

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220284992T>A (hg19) ; chr2:g.219420270T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420270T>A , CM000664.2:g.219420270T>A	GRCh38
NC_000002.11:g.220284992T>A , CM000664.1:g.220284992T>A	GRCh37
NC_000002.10:g.219993236T>A	NCBI36
NG_008043.1:g.6894T>A , LRG_380:g.6894T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.133T>A
ENST00000683013.1:n.47T>A
ENST00000373960.4:c.659T>A MANE Select	ENSP00000363071.3:p.Leu220Gln
ENST00000373960.3:c.659T>A	ENSP00000363071.3:p.Leu220Gln
ENST00000477226.5:n.131T>A
ENST00000492726.1:n.54T>A
NM_001927.3:c.659T>A , LRG_380t1:c.659T>A	NP_001918.3:p.Leu220Gln
NM_001927.4:c.659T>A MANE Select	NP_001918.3:p.Leu220Gln
NM_001382708.1:c.656T>A	NP_001369637.1:p.Leu219Gln
NM_001382709.1:c.659T>A	NP_001369638.1:p.Leu220Gln
NM_001382710.1:c.659T>A	NP_001369639.1:p.Leu220Gln
NM_001382711.1:c.659T>A	NP_001369640.1:p.Leu220Gln
NM_001382712.1:c.659T>A	NP_001369641.1:p.Leu220Gln
NM_001382713.1:c.496-255T>A	NP_001369642.1:n.496-255T>A