Canonical Allele Identifier: CA1329213027
Gene: DES HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219425510G= , CM000664.2:g.219425510G= GRCh38
NC_000002.11:g.220290232G= , CM000664.1:g.220290232G= GRCh37
NC_000002.10:g.219998476G= NCBI36
NG_008043.1:g.12134G= , LRG_380:g.12134G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000477226.6:n.763-153G=
ENST00000683013.1:n.677-153G=
ENST00000373960.4:c.1289-153G= MANE Select ENSP00000363071.3:n.1289-153G=
ENST00000373960.3:c.1289-153G= ENSP00000363071.3:n.1289-153G=
NM_001927.3:c.1289-153G= , LRG_380t1:c.1289-153G= NP_001918.3:n.1289-153G=
NM_001927.4:c.1289-153G= MANE Select NP_001918.3:n.1289-153G=
NM_001382708.1:c.1286-153G= NP_001369637.1:n.1286-153G=
NM_001382709.1:c.857-153G= NP_001369638.1:n.857-153G=
NM_001382710.1:c.1220-153G= NP_001369639.1:n.1220-153G=
NM_001382711.1:c.1268-153G= NP_001369640.1:n.1268-153G=
NM_001382712.1:c.1289-153G= NP_001369641.1:n.1289-153G=
NM_001382713.1:c.1019-153G= NP_001369642.1:n.1019-153G=