Canonical Allele Identifier: CA350699209

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220290704G>T (hg19) ; chr2:g.219425982G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219425982G>T , CM000664.2:g.219425982G>T	GRCh38
NC_000002.11:g.220290704G>T , CM000664.1:g.220290704G>T	GRCh37
NC_000002.10:g.219998948G>T	NCBI36
NG_008043.1:g.12606G>T , LRG_380:g.12606G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.879G>T
ENST00000683013.1:n.793G>T
ENST00000373960.4:c.1405G>T MANE Select	ENSP00000363071.3:p.Val469Leu
ENST00000373960.3:c.1405G>T	ENSP00000363071.3:p.Val469Leu
ENST00000483395.1:n.260G>T
NM_001927.3:c.1405G>T , LRG_380t1:c.1405G>T	NP_001918.3:p.Val469Leu
NM_001927.4:c.1405G>T MANE Select	NP_001918.3:p.Val469Leu
NM_001382708.1:c.1402G>T	NP_001369637.1:p.Val468Leu
NM_001382709.1:c.973G>T	NP_001369638.1:p.Val325Leu
NM_001382710.1:c.1336G>T	NP_001369639.1:p.Val446Leu
NM_001382711.1:c.1384G>T	NP_001369640.1:p.Val462Leu
NM_001382712.1:c.1371+237G>T	NP_001369641.1:n.1371+237G>T
NM_001382713.1:c.1135G>T	NP_001369642.1:p.Val379Leu