Canonical Allele Identifier: CA2663252145

Gene: DES

Linked Data

• gnomAD v4: 2-219425647-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425647A>G , CM000664.2:g.219425647A>G	GRCh38
NC_000002.11:g.220290369A>G , CM000664.1:g.220290369A>G	GRCh37
NC_000002.10:g.219998613A>G	NCBI36
NG_008043.1:g.12271A>G , LRG_380:g.12271A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.763-16A>G
ENST00000683013.1:n.677-16A>G
ENST00000373960.4:c.1289-16A>G MANE Select	ENSP00000363071.3:n.1289-16A>G
ENST00000373960.3:c.1289-16A>G	ENSP00000363071.3:n.1289-16A>G
ENST00000483395.1:n.128A>G
NM_001927.3:c.1289-16A>G , LRG_380t1:c.1289-16A>G	NP_001918.3:n.1289-16A>G
NM_001927.4:c.1289-16A>G MANE Select	NP_001918.3:n.1289-16A>G
NM_001382708.1:c.1286-16A>G	NP_001369637.1:n.1286-16A>G
NM_001382709.1:c.857-16A>G	NP_001369638.1:n.857-16A>G
NM_001382710.1:c.1220-16A>G	NP_001369639.1:n.1220-16A>G
NM_001382711.1:c.1268-16A>G	NP_001369640.1:n.1268-16A>G
NM_001382712.1:c.1289-16A>G	NP_001369641.1:n.1289-16A>G
NM_001382713.1:c.1019-16A>G	NP_001369642.1:n.1019-16A>G