Canonical Allele Identifier: CA350686018
Gene: DES HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219418879A>C , CM000664.2:g.219418879A>C GRCh38
NC_000002.11:g.220283601A>C , CM000664.1:g.220283601A>C GRCh37
NC_000002.10:g.219991845A>C NCBI36
NG_008043.1:g.5503A>C , LRG_380:g.5503A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000373960.4:c.417A>C MANE Select ENSP00000363071.3:p.Glu139Asp
ENST00000373960.3:c.417A>C ENSP00000363071.3:p.Glu139Asp
NM_001927.3:c.417A>C , LRG_380t1:c.417A>C NP_001918.3:p.Glu139Asp
NM_001927.4:c.417A>C MANE Select NP_001918.3:p.Glu139Asp
NM_001382708.1:c.417A>C NP_001369637.1:p.Glu139Asp
NM_001382709.1:c.417A>C NP_001369638.1:p.Glu139Asp
NM_001382710.1:c.417A>C NP_001369639.1:p.Glu139Asp
NM_001382711.1:c.417A>C NP_001369640.1:p.Glu139Asp
NM_001382712.1:c.417A>C NP_001369641.1:p.Glu139Asp
NM_001382713.1:c.417A>C NP_001369642.1:p.Glu139Asp