Canonical Allele Identifier: CA2663248093
Gene: DES HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219418396_219418397del , CM000664.2:g.219418396_219418397del GRCh38
NC_000002.11:g.220283118_220283119del , CM000664.1:g.220283118_220283119del GRCh37
NC_000002.10:g.219991362_219991363del NCBI36
NG_008043.1:g.5020_5021del , LRG_380:g.5020_5021del

Transcript Alleles

HGVS Amino-acid change
ENST00000373960.4:c.-67_-66del MANE Select ENSP00000363071.3:n.-67_-66del
ENST00000373960.3:c.-67_-66del ENSP00000363071.3:n.-67_-66del
NM_001927.3:c.-67_-66del , LRG_380t1:c.-67_-66del NP_001918.3:n.-67_-66del
NM_001927.4:c.-67_-66del MANE Select NP_001918.3:n.-67_-66del
NM_001382708.1:c.-67_-66del NP_001369637.1:n.-67_-66del
NM_001382709.1:c.-67_-66del NP_001369638.1:n.-67_-66del
NM_001382710.1:c.-67_-66del NP_001369639.1:n.-67_-66del
NM_001382711.1:c.-67_-66del NP_001369640.1:n.-67_-66del
NM_001382712.1:c.-67_-66del NP_001369641.1:n.-67_-66del
NM_001382713.1:c.-67_-66del NP_001369642.1:n.-67_-66del