Canonical Allele Identifier: CA1329210945

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420681G= , CM000664.2:g.219420681G=	GRCh38
NC_000002.11:g.220285403G= , CM000664.1:g.220285403G=	GRCh37
NC_000002.10:g.219993647G=	NCBI36
NG_008043.1:g.7305G= , LRG_380:g.7305G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.371+25G=
ENST00000683013.1:n.285+25G=
ENST00000373960.4:c.897+25G= MANE Select	ENSP00000363071.3:n.897+25G=
ENST00000373960.3:c.897+25G=	ENSP00000363071.3:n.897+25G=
ENST00000477226.5:n.369+25G=
ENST00000492726.1:n.292+25G=
NM_001927.3:c.897+25G= , LRG_380t1:c.897+25G=	NP_001918.3:n.897+25G=
NM_001927.4:c.897+25G= MANE Select	NP_001918.3:n.897+25G=
NM_001382708.1:c.894+25G=	NP_001369637.1:n.894+25G=
NM_001382709.1:c.735+335G=	NP_001369638.1:n.735+335G=
NM_001382710.1:c.897+25G=	NP_001369639.1:n.897+25G=
NM_001382711.1:c.897+25G=	NP_001369640.1:n.897+25G=
NM_001382712.1:c.897+25G=	NP_001369641.1:n.897+25G=
NM_001382713.1:c.627+25G=	NP_001369642.1:n.627+25G=