Canonical Allele Identifier: CA1329210881

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420551C= , CM000664.2:g.219420551C=	GRCh38
NC_000002.11:g.220285273C= , CM000664.1:g.220285273C=	GRCh37
NC_000002.10:g.219993517C=	NCBI36
NG_008043.1:g.7175C= , LRG_380:g.7175C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.266C=
ENST00000683013.1:n.180C=
ENST00000373960.4:c.792C= MANE Select	ENSP00000363071.3:p.Asp264=
ENST00000373960.3:c.792C=	ENSP00000363071.3:p.Asp264=
ENST00000477226.5:n.264C=
ENST00000492726.1:n.187C=
NM_001927.3:c.792C= , LRG_380t1:c.792C=	NP_001918.3:p.Asp264=
NM_001927.4:c.792C= MANE Select	NP_001918.3:p.Asp264=
NM_001382708.1:c.789C=	NP_001369637.1:p.Asp263=
NM_001382709.1:c.735+205C=	NP_001369638.1:n.735+205C=
NM_001382710.1:c.792C=	NP_001369639.1:p.Asp264=
NM_001382711.1:c.792C=	NP_001369640.1:p.Asp264=
NM_001382712.1:c.792C=	NP_001369641.1:p.Asp264=
NM_001382713.1:c.522C=	NP_001369642.1:p.Asp174=