Canonical Allele Identifier: CA1329211202
Gene: DES HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219421297T= , CM000664.2:g.219421297T= GRCh38
NC_000002.11:g.220286019T= , CM000664.1:g.220286019T= GRCh37
NC_000002.10:g.219994263T= NCBI36
NG_008043.1:g.7921T= , LRG_380:g.7921T=

Transcript Alleles

HGVS Amino-acid change
ENST00000477226.6:n.498-43T=
ENST00000683013.1:n.412-43T=
ENST00000373960.4:c.1024-43T= MANE Select ENSP00000363071.3:n.1024-43T=
ENST00000373960.3:c.1024-43T= ENSP00000363071.3:n.1024-43T=
ENST00000477226.5:n.496-43T=
ENST00000492726.1:n.419-43T=
NM_001927.3:c.1024-43T= , LRG_380t1:c.1024-43T= NP_001918.3:n.1024-43T=
NM_001927.4:c.1024-43T= MANE Select NP_001918.3:n.1024-43T=
NM_001382708.1:c.1021-43T= NP_001369637.1:n.1021-43T=
NM_001382709.1:c.736-187T= NP_001369638.1:n.736-187T=
NM_001382710.1:c.1024-112T= NP_001369639.1:n.1024-112T=
NM_001382711.1:c.1024-64T= NP_001369640.1:n.1024-64T=
NM_001382712.1:c.1024-43T= NP_001369641.1:n.1024-43T=
NM_001382713.1:c.754-43T= NP_001369642.1:n.754-43T=