Canonical Allele Identifier: CA539843111

Gene: DES

Linked Data

• dbSNP Id: rs1285197831
• gnomAD v2: 2-220284790-G-A
• gnomAD v4: 2-219420068-G-A
• MyVariant Identifiers: chr2:g.220284790G>A (hg19) ; chr2:g.219420068G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420068G>A , CM000664.2:g.219420068G>A	GRCh38
NC_000002.11:g.220284790G>A , CM000664.1:g.220284790G>A	GRCh37
NC_000002.10:g.219993034G>A	NCBI36
NG_008043.1:g.6692G>A , LRG_380:g.6692G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.26G>A
ENST00000373960.4:c.579-27G>A MANE Select	ENSP00000363071.3:n.579-27G>A
ENST00000373960.3:c.579-27G>A	ENSP00000363071.3:n.579-27G>A
ENST00000477226.5:n.24G>A
NM_001927.3:c.579-27G>A , LRG_380t1:c.579-27G>A	NP_001918.3:n.579-27G>A
NM_001927.4:c.579-27G>A MANE Select	NP_001918.3:n.579-27G>A
NM_001382708.1:c.579-27G>A	NP_001369637.1:n.579-27G>A
NM_001382709.1:c.579-27G>A	NP_001369638.1:n.579-27G>A
NM_001382710.1:c.579-27G>A	NP_001369639.1:n.579-27G>A
NM_001382711.1:c.579-27G>A	NP_001369640.1:n.579-27G>A
NM_001382712.1:c.579-27G>A	NP_001369641.1:n.579-27G>A
NM_001382713.1:c.496-457G>A	NP_001369642.1:n.496-457G>A