Canonical Allele Identifier: CA1329210673
Gene: DES HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219420172T= , CM000664.2:g.219420172T= GRCh38
NC_000002.11:g.220284894T= , CM000664.1:g.220284894T= GRCh37
NC_000002.10:g.219993138T= NCBI36
NG_008043.1:g.6796T= , LRG_380:g.6796T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477226.6:n.113+17T=
ENST00000373960.4:c.639+17T= MANE Select ENSP00000363071.3:n.639+17T=
ENST00000373960.3:c.639+17T= ENSP00000363071.3:n.639+17T=
ENST00000477226.5:n.111+17T=
ENST00000492726.1:n.34+17T=
NM_001927.3:c.639+17T= , LRG_380t1:c.639+17T= NP_001918.3:n.639+17T=
NM_001927.4:c.639+17T= MANE Select NP_001918.3:n.639+17T=
NM_001382708.1:c.636+20T= NP_001369637.1:n.636+20T=
NM_001382709.1:c.639+17T= NP_001369638.1:n.639+17T=
NM_001382710.1:c.639+17T= NP_001369639.1:n.639+17T=
NM_001382711.1:c.639+17T= NP_001369640.1:n.639+17T=
NM_001382712.1:c.639+17T= NP_001369641.1:n.639+17T=
NM_001382713.1:c.496-353T= NP_001369642.1:n.496-353T=