Canonical Allele Identifier: CA2839578734

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425588del , CM000664.2:g.219425588del	GRCh38
NC_000002.11:g.220290310del , CM000664.1:g.220290310del	GRCh37
NC_000002.10:g.219998554del	NCBI36
NG_008043.1:g.12212del , LRG_380:g.12212del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.763-75del
ENST00000683013.1:n.677-75del
ENST00000373960.4:c.1289-75del MANE Select	ENSP00000363071.3:n.1289-75del
ENST00000373960.3:c.1289-75del	ENSP00000363071.3:n.1289-75del
ENST00000483395.1:n.69del
NM_001927.3:c.1289-75del , LRG_380t1:c.1289-75del	NP_001918.3:n.1289-75del
NM_001927.4:c.1289-75del MANE Select	NP_001918.3:n.1289-75del
NM_001382708.1:c.1286-75del	NP_001369637.1:n.1286-75del
NM_001382709.1:c.857-75del	NP_001369638.1:n.857-75del
NM_001382710.1:c.1220-75del	NP_001369639.1:n.1220-75del
NM_001382711.1:c.1268-75del	NP_001369640.1:n.1268-75del
NM_001382712.1:c.1289-75del	NP_001369641.1:n.1289-75del
NM_001382713.1:c.1019-75del	NP_001369642.1:n.1019-75del