Canonical Allele Identifier: CA1329211268

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421409G= , CM000664.2:g.219421409G=	GRCh38
NC_000002.11:g.220286131G= , CM000664.1:g.220286131G=	GRCh37
NC_000002.10:g.219994375G=	NCBI36
NG_008043.1:g.8033G= , LRG_380:g.8033G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.567G=
ENST00000683013.1:n.481G=
ENST00000373960.4:c.1093G= MANE Select	ENSP00000363071.3:p.Asp365=
ENST00000373960.3:c.1093G=	ENSP00000363071.3:p.Asp365=
ENST00000477226.5:n.565G=
ENST00000492726.1:n.488G=
NM_001927.3:c.1093G= , LRG_380t1:c.1093G=	NP_001918.3:p.Asp365=
NM_001927.4:c.1093G= MANE Select	NP_001918.3:p.Asp365=
NM_001382708.1:c.1090G=	NP_001369637.1:p.Asp364=
NM_001382709.1:c.736-75G=	NP_001369638.1:n.736-75G=
NM_001382710.1:c.1024G=	NP_001369639.1:p.Asp342=
NM_001382711.1:c.1072G=	NP_001369640.1:p.Asp358=
NM_001382712.1:c.1093G=	NP_001369641.1:p.Asp365=
NM_001382713.1:c.823G=	NP_001369642.1:p.Asp275=