Canonical Allele Identifier: CA350698500

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220290419T>A (hg19) ; chr2:g.219425697T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425697T>A , CM000664.2:g.219425697T>A	GRCh38
NC_000002.11:g.220290419T>A , CM000664.1:g.220290419T>A	GRCh37
NC_000002.10:g.219998663T>A	NCBI36
NG_008043.1:g.12321T>A , LRG_380:g.12321T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.797T>A
ENST00000683013.1:n.711T>A
ENST00000373960.4:c.1323T>A MANE Select	ENSP00000363071.3:p.His441Gln
ENST00000373960.3:c.1323T>A	ENSP00000363071.3:p.His441Gln
ENST00000483395.1:n.178T>A
NM_001927.3:c.1323T>A , LRG_380t1:c.1323T>A	NP_001918.3:p.His441Gln
NM_001927.4:c.1323T>A MANE Select	NP_001918.3:p.His441Gln
NM_001382708.1:c.1320T>A	NP_001369637.1:p.His440Gln
NM_001382709.1:c.891T>A	NP_001369638.1:p.His297Gln
NM_001382710.1:c.1254T>A	NP_001369639.1:p.His418Gln
NM_001382711.1:c.1302T>A	NP_001369640.1:p.His434Gln
NM_001382712.1:c.1323T>A	NP_001369641.1:p.His441Gln
NM_001382713.1:c.1053T>A	NP_001369642.1:p.His351Gln