Canonical Allele Identifier: CA2663247846

Gene: DES

Linked Data

• gnomAD v4: 2-219419083-CACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219419084_219419086del , CM000664.2:g.219419084_219419086del	GRCh38
NC_000002.11:g.220283806_220283808del , CM000664.1:g.220283806_220283808del	GRCh37
NC_000002.10:g.219992050_219992052del	NCBI36
NG_008043.1:g.5708_5710del , LRG_380:g.5708_5710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373960.4:c.578+44_578+46del MANE Select	ENSP00000363071.3:n.578+44_578+46del
ENST00000373960.3:c.578+44_578+46del	ENSP00000363071.3:n.578+44_578+46del
NM_001927.3:c.578+44_578+46del , LRG_380t1:c.578+44_578+46del	NP_001918.3:n.578+44_578+46del
NM_001927.4:c.578+44_578+46del MANE Select	NP_001918.3:n.578+44_578+46del
NM_001382708.1:c.578+44_578+46del	NP_001369637.1:n.578+44_578+46del
NM_001382709.1:c.578+44_578+46del	NP_001369638.1:n.578+44_578+46del
NM_001382710.1:c.578+44_578+46del	NP_001369639.1:n.578+44_578+46del
NM_001382711.1:c.578+44_578+46del	NP_001369640.1:n.578+44_578+46del
NM_001382712.1:c.578+44_578+46del	NP_001369641.1:n.578+44_578+46del
NM_001382713.1:c.495+127_495+129del	NP_001369642.1:n.495+127_495+129del