Canonical Allele Identifier: CA1329213402
Gene: DES HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219426333C= , CM000664.2:g.219426333C= GRCh38
NC_000002.11:g.220291055C= , CM000664.1:g.220291055C= GRCh37
NC_000002.10:g.219999299C= NCBI36
NG_008043.1:g.12957C= , LRG_380:g.12957C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477226.6:n.1230C=
ENST00000683013.1:n.1144C=
ENST00000373960.4:c.*343C= MANE Select ENSP00000363071.3:n.*343C=
ENST00000373960.3:c.*343C= ENSP00000363071.3:n.*343C=
NM_001927.3:c.*343C= , LRG_380t1:c.*343C= NP_001918.3:n.*343C=
NM_001927.4:c.*343C= MANE Select NP_001918.3:n.*343C=
NM_001382708.1:c.*343C= NP_001369637.1:n.*343C=
NM_001382709.1:c.*343C= NP_001369638.1:n.*343C=
NM_001382710.1:c.*343C= NP_001369639.1:n.*343C=
NM_001382711.1:c.*343C= NP_001369640.1:n.*343C=
NM_001382712.1:c.1372-220C= NP_001369641.1:n.1372-220C=
NM_001382713.1:c.*343C= NP_001369642.1:n.*343C=