Canonical Allele Identifier: CA1329211326

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421502A= , CM000664.2:g.219421502A=	GRCh38
NC_000002.11:g.220286224A= , CM000664.1:g.220286224A=	GRCh37
NC_000002.10:g.219994468A=	NCBI36
NG_008043.1:g.8126A= , LRG_380:g.8126A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.660A=
ENST00000683013.1:n.574A=
ENST00000373960.4:c.1186A= MANE Select	ENSP00000363071.3:p.Met396=
ENST00000373960.3:c.1186A=	ENSP00000363071.3:p.Met396=
ENST00000477226.5:n.658A=
ENST00000492726.1:n.581A=
NM_001927.3:c.1186A= , LRG_380t1:c.1186A=	NP_001918.3:p.Met396=
NM_001927.4:c.1186A= MANE Select	NP_001918.3:p.Met396=
NM_001382708.1:c.1183A=	NP_001369637.1:p.Met395=
NM_001382709.1:c.754A=	NP_001369638.1:p.Met252=
NM_001382710.1:c.1117A=	NP_001369639.1:p.Met373=
NM_001382711.1:c.1165A=	NP_001369640.1:p.Met389=
NM_001382712.1:c.1186A=	NP_001369641.1:p.Met396=
NM_001382713.1:c.916A=	NP_001369642.1:p.Met306=