Canonical Allele Identifier: CA350699093
Gene: DES HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219425971A>T , CM000664.2:g.219425971A>T GRCh38
NC_000002.11:g.220290693A>T , CM000664.1:g.220290693A>T GRCh37
NC_000002.10:g.219998937A>T NCBI36
NG_008043.1:g.12595A>T , LRG_380:g.12595A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000477226.6:n.868A>T
ENST00000683013.1:n.782A>T
ENST00000373960.4:c.1394A>T MANE Select ENSP00000363071.3:p.Gln465Leu
ENST00000373960.3:c.1394A>T ENSP00000363071.3:p.Gln465Leu
ENST00000483395.1:n.249A>T
NM_001927.3:c.1394A>T , LRG_380t1:c.1394A>T NP_001918.3:p.Gln465Leu
NM_001927.4:c.1394A>T MANE Select NP_001918.3:p.Gln465Leu
NM_001382708.1:c.1391A>T NP_001369637.1:p.Gln464Leu
NM_001382709.1:c.962A>T NP_001369638.1:p.Gln321Leu
NM_001382710.1:c.1325A>T NP_001369639.1:p.Gln442Leu
NM_001382711.1:c.1373A>T NP_001369640.1:p.Gln458Leu
NM_001382712.1:c.1371+226A>T NP_001369641.1:n.1371+226A>T
NM_001382713.1:c.1124A>T NP_001369642.1:p.Gln375Leu