Canonical Allele Identifier: CA10603828

Gene: DES

Linked Data

• ClinVar Variation Id: 281234
• ClinVar RCV Id: RCV000489159 ; RCV001321146
• dbSNP Id: rs267607486
• MyVariant Identifiers: chr2:g.220285068G>A (hg19) ; chr2:g.219420346G>A (hg38)
• PubMed: PMID:23891399

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420346G>A , CM000664.2:g.219420346G>A	GRCh38
NC_000002.11:g.220285068G>A , CM000664.1:g.220285068G>A	GRCh37
NC_000002.10:g.219993312G>A	NCBI36
NG_008043.1:g.6970G>A , LRG_380:g.6970G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.209G>A
ENST00000683013.1:n.123G>A
ENST00000373960.4:c.735G>A MANE Select	ENSP00000363071.3:p.Glu245=
ENST00000373960.3:c.735G>A	ENSP00000363071.3:p.Glu245=
ENST00000477226.5:n.207G>A
ENST00000492726.1:n.130G>A
NM_001927.3:c.735G>A , LRG_380t1:c.735G>A	NP_001918.3:p.Glu245=
NM_001927.4:c.735G>A MANE Select	NP_001918.3:p.Glu245=
NM_001382708.1:c.732G>A	NP_001369637.1:p.Glu244=
NM_001382709.1:c.735G>A	NP_001369638.1:p.Glu245=
NM_001382710.1:c.735G>A	NP_001369639.1:p.Glu245=
NM_001382711.1:c.735G>A	NP_001369640.1:p.Glu245=
NM_001382712.1:c.735G>A	NP_001369641.1:p.Glu245=
NM_001382713.1:c.496-179G>A	NP_001369642.1:n.496-179G>A