Canonical Allele Identifier: CA1329213191

Gene: DES

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425857A= , CM000664.2:g.219425857A=	GRCh38
NC_000002.11:g.220290579A= , CM000664.1:g.220290579A=	GRCh37
NC_000002.10:g.219998823A=	NCBI36
NG_008043.1:g.12481A= , LRG_380:g.12481A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.846-92A=
ENST00000683013.1:n.760-92A=
ENST00000373960.4:c.1372-92A= MANE Select	ENSP00000363071.3:n.1372-92A=
ENST00000373960.3:c.1372-92A=	ENSP00000363071.3:n.1372-92A=
ENST00000483395.1:n.227-92A=
NM_001927.3:c.1372-92A= , LRG_380t1:c.1372-92A=	NP_001918.3:n.1372-92A=
NM_001927.4:c.1372-92A= MANE Select	NP_001918.3:n.1372-92A=
NM_001382708.1:c.1369-92A=	NP_001369637.1:n.1369-92A=
NM_001382709.1:c.940-92A=	NP_001369638.1:n.940-92A=
NM_001382710.1:c.1303-92A=	NP_001369639.1:n.1303-92A=
NM_001382711.1:c.1351-92A=	NP_001369640.1:n.1351-92A=
NM_001382712.1:c.1371+112A=	NP_001369641.1:n.1371+112A=
NM_001382713.1:c.1102-92A=	NP_001369642.1:n.1102-92A=