Canonical Allele Identifier: CA350685468
Gene: DES HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219418817T>G , CM000664.2:g.219418817T>G GRCh38
NC_000002.11:g.220283539T>G , CM000664.1:g.220283539T>G GRCh37
NC_000002.10:g.219991783T>G NCBI36
NG_008043.1:g.5441T>G , LRG_380:g.5441T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000373960.4:c.355T>G MANE Select ENSP00000363071.3:p.Phe119Val
ENST00000373960.3:c.355T>G ENSP00000363071.3:p.Phe119Val
NM_001927.3:c.355T>G , LRG_380t1:c.355T>G NP_001918.3:p.Phe119Val
NM_001927.4:c.355T>G MANE Select NP_001918.3:p.Phe119Val
NM_001382708.1:c.355T>G NP_001369637.1:p.Phe119Val
NM_001382709.1:c.355T>G NP_001369638.1:p.Phe119Val
NM_001382710.1:c.355T>G NP_001369639.1:p.Phe119Val
NM_001382711.1:c.355T>G NP_001369640.1:p.Phe119Val
NM_001382712.1:c.355T>G NP_001369641.1:p.Phe119Val
NM_001382713.1:c.355T>G NP_001369642.1:p.Phe119Val