Canonical Allele Identifier: CA2663250548

Gene: DES

Linked Data

• gnomAD v4: 2-219421565-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421565G>A , CM000664.2:g.219421565G>A	GRCh38
NC_000002.11:g.220286287G>A , CM000664.1:g.220286287G>A	GRCh37
NC_000002.10:g.219994531G>A	NCBI36
NG_008043.1:g.8189G>A , LRG_380:g.8189G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.718+5G>A
ENST00000683013.1:n.632+5G>A
ENST00000373960.4:c.1244+5G>A MANE Select	ENSP00000363071.3:n.1244+5G>A
ENST00000373960.3:c.1244+5G>A	ENSP00000363071.3:n.1244+5G>A
ENST00000477226.5:n.716+5G>A
ENST00000492726.1:n.639+5G>A
NM_001927.3:c.1244+5G>A , LRG_380t1:c.1244+5G>A	NP_001918.3:n.1244+5G>A
NM_001927.4:c.1244+5G>A MANE Select	NP_001918.3:n.1244+5G>A
NM_001382708.1:c.1241+5G>A	NP_001369637.1:n.1241+5G>A
NM_001382709.1:c.812+5G>A	NP_001369638.1:n.812+5G>A
NM_001382710.1:c.1175+5G>A	NP_001369639.1:n.1175+5G>A
NM_001382711.1:c.1223+5G>A	NP_001369640.1:n.1223+5G>A
NM_001382712.1:c.1244+5G>A	NP_001369641.1:n.1244+5G>A
NM_001382713.1:c.974+5G>A	NP_001369642.1:n.974+5G>A