Canonical Allele Identifier: CA1329211214
Gene: DES HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219421321G= , CM000664.2:g.219421321G= GRCh38
NC_000002.11:g.220286043G= , CM000664.1:g.220286043G= GRCh37
NC_000002.10:g.219994287G= NCBI36
NG_008043.1:g.7945G= , LRG_380:g.7945G=

Transcript Alleles

HGVS Amino-acid change
ENST00000477226.6:n.498-19G=
ENST00000683013.1:n.412-19G=
ENST00000373960.4:c.1024-19G= MANE Select ENSP00000363071.3:n.1024-19G=
ENST00000373960.3:c.1024-19G= ENSP00000363071.3:n.1024-19G=
ENST00000477226.5:n.496-19G=
ENST00000492726.1:n.419-19G=
NM_001927.3:c.1024-19G= , LRG_380t1:c.1024-19G= NP_001918.3:n.1024-19G=
NM_001927.4:c.1024-19G= MANE Select NP_001918.3:n.1024-19G=
NM_001382708.1:c.1021-19G= NP_001369637.1:n.1021-19G=
NM_001382709.1:c.736-163G= NP_001369638.1:n.736-163G=
NM_001382710.1:c.1024-88G= NP_001369639.1:n.1024-88G=
NM_001382711.1:c.1024-40G= NP_001369640.1:n.1024-40G=
NM_001382712.1:c.1024-19G= NP_001369641.1:n.1024-19G=
NM_001382713.1:c.754-19G= NP_001369642.1:n.754-19G=