Canonical Allele Identifier: CA1329210139

Gene: DES

Linked Data

• dbSNP Id: rs1954380845

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219418996_219419010del , CM000664.2:g.219418996_219419010del	GRCh38
NC_000002.11:g.220283718_220283732del , CM000664.1:g.220283718_220283732del	GRCh37
NC_000002.10:g.219991962_219991976del	NCBI36
NG_008043.1:g.5620_5634del , LRG_380:g.5620_5634del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373960.4:c.534_548del MANE Select	ENSP00000363071.3:p.Glu179_Leu183del
ENST00000373960.3:c.534_548del	ENSP00000363071.3:p.Glu179_Leu183del
NM_001927.3:c.534_548del , LRG_380t1:c.534_548del	NP_001918.3:p.Glu179_Leu183del
NM_001927.4:c.534_548del MANE Select	NP_001918.3:p.Glu179_Leu183del
NM_001382708.1:c.534_548del	NP_001369637.1:p.Glu179_Leu183del
NM_001382709.1:c.534_548del	NP_001369638.1:p.Glu179_Leu183del
NM_001382710.1:c.534_548del	NP_001369639.1:p.Glu179_Leu183del
NM_001382711.1:c.534_548del	NP_001369640.1:p.Glu179_Leu183del
NM_001382712.1:c.534_548del	NP_001369641.1:p.Glu179_Leu183del
NM_001382713.1:c.495+39_495+53del	NP_001369642.1:n.495+39_495+53del