Canonical Allele Identifier: CA1329210682
Gene: DES HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219420182T= , CM000664.2:g.219420182T= GRCh38
NC_000002.11:g.220284904T= , CM000664.1:g.220284904T= GRCh37
NC_000002.10:g.219993148T= NCBI36
NG_008043.1:g.6806T= , LRG_380:g.6806T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477226.6:n.113+27T=
ENST00000373960.4:c.639+27T= MANE Select ENSP00000363071.3:n.639+27T=
ENST00000373960.3:c.639+27T= ENSP00000363071.3:n.639+27T=
ENST00000477226.5:n.111+27T=
ENST00000492726.1:n.34+27T=
NM_001927.3:c.639+27T= , LRG_380t1:c.639+27T= NP_001918.3:n.639+27T=
NM_001927.4:c.639+27T= MANE Select NP_001918.3:n.639+27T=
NM_001382708.1:c.636+30T= NP_001369637.1:n.636+30T=
NM_001382709.1:c.639+27T= NP_001369638.1:n.639+27T=
NM_001382710.1:c.639+27T= NP_001369639.1:n.639+27T=
NM_001382711.1:c.639+27T= NP_001369640.1:n.639+27T=
NM_001382712.1:c.639+27T= NP_001369641.1:n.639+27T=
NM_001382713.1:c.496-343T= NP_001369642.1:n.496-343T=