Canonical Allele Identifier: CA1329210060
Gene: DES HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219418885C= , CM000664.2:g.219418885C= GRCh38
NC_000002.11:g.220283607C= , CM000664.1:g.220283607C= GRCh37
NC_000002.10:g.219991851C= NCBI36
NG_008043.1:g.5509C= , LRG_380:g.5509C=

Transcript Alleles

HGVS Amino-acid change
ENST00000373960.4:c.423C= MANE Select ENSP00000363071.3:p.Asn141=
ENST00000373960.3:c.423C= ENSP00000363071.3:p.Asn141=
NM_001927.3:c.423C= , LRG_380t1:c.423C= NP_001918.3:p.Asn141=
NM_001927.4:c.423C= MANE Select NP_001918.3:p.Asn141=
NM_001382708.1:c.423C= NP_001369637.1:p.Asn141=
NM_001382709.1:c.423C= NP_001369638.1:p.Asn141=
NM_001382710.1:c.423C= NP_001369639.1:p.Asn141=
NM_001382711.1:c.423C= NP_001369640.1:p.Asn141=
NM_001382712.1:c.423C= NP_001369641.1:p.Asn141=
NM_001382713.1:c.423C= NP_001369642.1:p.Asn141=