Canonical Allele Identifier: CA350685407
Gene: DES HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219418808A>T , CM000664.2:g.219418808A>T GRCh38
NC_000002.11:g.220283530A>T , CM000664.1:g.220283530A>T GRCh37
NC_000002.10:g.219991774A>T NCBI36
NG_008043.1:g.5432A>T , LRG_380:g.5432A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000373960.4:c.346A>T MANE Select ENSP00000363071.3:p.Asn116Tyr
ENST00000373960.3:c.346A>T ENSP00000363071.3:p.Asn116Tyr
NM_001927.3:c.346A>T , LRG_380t1:c.346A>T NP_001918.3:p.Asn116Tyr
NM_001927.4:c.346A>T MANE Select NP_001918.3:p.Asn116Tyr
NM_001382708.1:c.346A>T NP_001369637.1:p.Asn116Tyr
NM_001382709.1:c.346A>T NP_001369638.1:p.Asn116Tyr
NM_001382710.1:c.346A>T NP_001369639.1:p.Asn116Tyr
NM_001382711.1:c.346A>T NP_001369640.1:p.Asn116Tyr
NM_001382712.1:c.346A>T NP_001369641.1:p.Asn116Tyr
NM_001382713.1:c.346A>T NP_001369642.1:p.Asn116Tyr