Canonical Allele Identifier: CA1329211155

Gene: DES

Linked Data

• dbSNP Id: rs1954433709

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421178G>A , CM000664.2:g.219421178G>A	GRCh38
NC_000002.11:g.220285900G>A , CM000664.1:g.220285900G>A	GRCh37
NC_000002.10:g.219994144G>A	NCBI36
NG_008043.1:g.7802G>A , LRG_380:g.7802G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.498-162G>A
ENST00000683013.1:n.412-162G>A
ENST00000373960.4:c.1024-162G>A MANE Select	ENSP00000363071.3:n.1024-162G>A
ENST00000373960.3:c.1024-162G>A	ENSP00000363071.3:n.1024-162G>A
ENST00000477226.5:n.496-162G>A
ENST00000492726.1:n.419-162G>A
NM_001927.3:c.1024-162G>A , LRG_380t1:c.1024-162G>A	NP_001918.3:n.1024-162G>A
NM_001927.4:c.1024-162G>A MANE Select	NP_001918.3:n.1024-162G>A
NM_001382708.1:c.1021-162G>A	NP_001369637.1:n.1021-162G>A
NM_001382709.1:c.736-306G>A	NP_001369638.1:n.736-306G>A
NM_001382710.1:c.1023+225G>A	NP_001369639.1:n.1023+225G>A
NM_001382711.1:c.1024-183G>A	NP_001369640.1:n.1024-183G>A
NM_001382712.1:c.1024-162G>A	NP_001369641.1:n.1024-162G>A
NM_001382713.1:c.754-162G>A	NP_001369642.1:n.754-162G>A