Canonical Allele Identifier: CA431284513

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286281C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421559C>A , CM000664.2:g.219421559C>A	GRCh38
NC_000002.11:g.220286281C>A , CM000664.1:g.220286281C>A	GRCh37
NC_000002.10:g.219994525C>A	NCBI36
NG_008043.1:g.8183C>A , LRG_380:g.8183C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.717C>A
ENST00000683013.1:n.631C>A
ENST00000373960.4:c.1243C>A MANE Select	ENSP00000363071.3:p.Arg415=
ENST00000373960.3:c.1243C>A	ENSP00000363071.3:p.Arg415=
ENST00000477226.5:n.715C>A
ENST00000492726.1:n.638C>A
NM_001927.3:c.1243C>A , LRG_380t1:c.1243C>A	NP_001918.3:p.Arg415=
NM_001927.4:c.1243C>A MANE Select	NP_001918.3:p.Arg415=
NM_001382708.1:c.1240C>A	NP_001369637.1:p.Arg414=
NM_001382709.1:c.811C>A	NP_001369638.1:p.Arg271=
NM_001382710.1:c.1174C>A	NP_001369639.1:p.Arg392=
NM_001382711.1:c.1222C>A	NP_001369640.1:p.Arg408=
NM_001382712.1:c.1243C>A	NP_001369641.1:p.Arg415=
NM_001382713.1:c.973C>A	NP_001369642.1:p.Arg325=