Canonical Allele Identifier: CA1329211314

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421482A= , CM000664.2:g.219421482A=	GRCh38
NC_000002.11:g.220286204A= , CM000664.1:g.220286204A=	GRCh37
NC_000002.10:g.219994448A=	NCBI36
NG_008043.1:g.8106A= , LRG_380:g.8106A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.640A=
ENST00000683013.1:n.554A=
ENST00000373960.4:c.1166A= MANE Select	ENSP00000363071.3:p.Gln389=
ENST00000373960.3:c.1166A=	ENSP00000363071.3:p.Gln389=
ENST00000477226.5:n.638A=
ENST00000492726.1:n.561A=
NM_001927.3:c.1166A= , LRG_380t1:c.1166A=	NP_001918.3:p.Gln389=
NM_001927.4:c.1166A= MANE Select	NP_001918.3:p.Gln389=
NM_001382708.1:c.1163A=	NP_001369637.1:p.Gln388=
NM_001382709.1:c.736-2A=	NP_001369638.1:n.736-2A=
NM_001382710.1:c.1097A=	NP_001369639.1:p.Gln366=
NM_001382711.1:c.1145A=	NP_001369640.1:p.Gln382=
NM_001382712.1:c.1166A=	NP_001369641.1:p.Gln389=
NM_001382713.1:c.896A=	NP_001369642.1:p.Gln299=