Canonical Allele Identifier: CA350694284

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286149G>A (hg19) ; chr2:g.219421427G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421427G>A , CM000664.2:g.219421427G>A	GRCh38
NC_000002.11:g.220286149G>A , CM000664.1:g.220286149G>A	GRCh37
NC_000002.10:g.219994393G>A	NCBI36
NG_008043.1:g.8051G>A , LRG_380:g.8051G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.585G>A
ENST00000683013.1:n.499G>A
ENST00000373960.4:c.1111G>A MANE Select	ENSP00000363071.3:p.Glu371Lys
ENST00000373960.3:c.1111G>A	ENSP00000363071.3:p.Glu371Lys
ENST00000477226.5:n.583G>A
ENST00000492726.1:n.506G>A
NM_001927.3:c.1111G>A , LRG_380t1:c.1111G>A	NP_001918.3:p.Glu371Lys
NM_001927.4:c.1111G>A MANE Select	NP_001918.3:p.Glu371Lys
NM_001382708.1:c.1108G>A	NP_001369637.1:p.Glu370Lys
NM_001382709.1:c.736-57G>A	NP_001369638.1:n.736-57G>A
NM_001382710.1:c.1042G>A	NP_001369639.1:p.Glu348Lys
NM_001382711.1:c.1090G>A	NP_001369640.1:p.Glu364Lys
NM_001382712.1:c.1111G>A	NP_001369641.1:p.Glu371Lys
NM_001382713.1:c.841G>A	NP_001369642.1:p.Glu281Lys