Canonical Allele Identifier: CA350691670

Gene: DES

Linked Data

• ClinVar Variation Id: 1677711
• ClinVar RCV Id: RCV002224453 ; RCV004047210
• dbSNP Id: rs1954421395
• gnomAD v4: 2-219420623-C-A
• MyVariant Identifiers: chr2:g.220285345C>A (hg19) ; chr2:g.219420623C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420623C>A , CM000664.2:g.219420623C>A	GRCh38
NC_000002.11:g.220285345C>A , CM000664.1:g.220285345C>A	GRCh37
NC_000002.10:g.219993589C>A	NCBI36
NG_008043.1:g.7247C>A , LRG_380:g.7247C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.338C>A
ENST00000683013.1:n.252C>A
ENST00000373960.4:c.864C>A MANE Select	ENSP00000363071.3:p.Asn288Lys
ENST00000373960.3:c.864C>A	ENSP00000363071.3:p.Asn288Lys
ENST00000477226.5:n.336C>A
ENST00000492726.1:n.259C>A
NM_001927.3:c.864C>A , LRG_380t1:c.864C>A	NP_001918.3:p.Asn288Lys
NM_001927.4:c.864C>A MANE Select	NP_001918.3:p.Asn288Lys
NM_001382708.1:c.861C>A	NP_001369637.1:p.Asn287Lys
NM_001382709.1:c.735+277C>A	NP_001369638.1:n.735+277C>A
NM_001382710.1:c.864C>A	NP_001369639.1:p.Asn288Lys
NM_001382711.1:c.864C>A	NP_001369640.1:p.Asn288Lys
NM_001382712.1:c.864C>A	NP_001369641.1:p.Asn288Lys
NM_001382713.1:c.594C>A	NP_001369642.1:p.Asn198Lys