Canonical Allele Identifier: CA2663248108
Gene: DES HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219418400_219418401del , CM000664.2:g.219418400_219418401del GRCh38
NC_000002.11:g.220283122_220283123del , CM000664.1:g.220283122_220283123del GRCh37
NC_000002.10:g.219991366_219991367del NCBI36
NG_008043.1:g.5024_5025del , LRG_380:g.5024_5025del

Transcript Alleles

HGVS Amino-acid change
ENST00000373960.4:c.-63_-62del MANE Select ENSP00000363071.3:n.-63_-62del
ENST00000373960.3:c.-63_-62del ENSP00000363071.3:n.-63_-62del
NM_001927.3:c.-63_-62del , LRG_380t1:c.-63_-62del NP_001918.3:n.-63_-62del
NM_001927.4:c.-63_-62del MANE Select NP_001918.3:n.-63_-62del
NM_001382708.1:c.-63_-62del NP_001369637.1:n.-63_-62del
NM_001382709.1:c.-63_-62del NP_001369638.1:n.-63_-62del
NM_001382710.1:c.-63_-62del NP_001369639.1:n.-63_-62del
NM_001382711.1:c.-63_-62del NP_001369640.1:n.-63_-62del
NM_001382712.1:c.-63_-62del NP_001369641.1:n.-63_-62del
NM_001382713.1:c.-63_-62del NP_001369642.1:n.-63_-62del