Canonical Allele Identifier: CA1329211321

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421494A= , CM000664.2:g.219421494A=	GRCh38
NC_000002.11:g.220286216A= , CM000664.1:g.220286216A=	GRCh37
NC_000002.10:g.219994460A=	NCBI36
NG_008043.1:g.8118A= , LRG_380:g.8118A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.652A=
ENST00000683013.1:n.566A=
ENST00000373960.4:c.1178A= MANE Select	ENSP00000363071.3:p.Asn393=
ENST00000373960.3:c.1178A=	ENSP00000363071.3:p.Asn393=
ENST00000477226.5:n.650A=
ENST00000492726.1:n.573A=
NM_001927.3:c.1178A= , LRG_380t1:c.1178A=	NP_001918.3:p.Asn393=
NM_001927.4:c.1178A= MANE Select	NP_001918.3:p.Asn393=
NM_001382708.1:c.1175A=	NP_001369637.1:p.Asn392=
NM_001382709.1:c.746A=	NP_001369638.1:p.Asn249=
NM_001382710.1:c.1109A=	NP_001369639.1:p.Asn370=
NM_001382711.1:c.1157A=	NP_001369640.1:p.Asn386=
NM_001382712.1:c.1178A=	NP_001369641.1:p.Asn393=
NM_001382713.1:c.908A=	NP_001369642.1:p.Asn303=