Canonical Allele Identifier: CA1329210150

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219419007A= , CM000664.2:g.219419007A=	GRCh38
NC_000002.11:g.220283729A= , CM000664.1:g.220283729A=	GRCh37
NC_000002.10:g.219991973A=	NCBI36
NG_008043.1:g.5631A= , LRG_380:g.5631A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373960.4:c.545A= MANE Select	ENSP00000363071.3:p.Asn182=
ENST00000373960.3:c.545A=	ENSP00000363071.3:p.Asn182=
NM_001927.3:c.545A= , LRG_380t1:c.545A=	NP_001918.3:p.Asn182=
NM_001927.4:c.545A= MANE Select	NP_001918.3:p.Asn182=
NM_001382708.1:c.545A=	NP_001369637.1:p.Asn182=
NM_001382709.1:c.545A=	NP_001369638.1:p.Asn182=
NM_001382710.1:c.545A=	NP_001369639.1:p.Asn182=
NM_001382711.1:c.545A=	NP_001369640.1:p.Asn182=
NM_001382712.1:c.545A=	NP_001369641.1:p.Asn182=
NM_001382713.1:c.495+50A=	NP_001369642.1:n.495+50A=