Canonical Allele Identifier: CA350694976

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286244T>G (hg19) ; chr2:g.219421522T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421522T>G , CM000664.2:g.219421522T>G	GRCh38
NC_000002.11:g.220286244T>G , CM000664.1:g.220286244T>G	GRCh37
NC_000002.10:g.219994488T>G	NCBI36
NG_008043.1:g.8146T>G , LRG_380:g.8146T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.680T>G
ENST00000683013.1:n.594T>G
ENST00000373960.4:c.1206T>G MANE Select	ENSP00000363071.3:p.Ile402Met
ENST00000373960.3:c.1206T>G	ENSP00000363071.3:p.Ile402Met
ENST00000477226.5:n.678T>G
ENST00000492726.1:n.601T>G
NM_001927.3:c.1206T>G , LRG_380t1:c.1206T>G	NP_001918.3:p.Ile402Met
NM_001927.4:c.1206T>G MANE Select	NP_001918.3:p.Ile402Met
NM_001382708.1:c.1203T>G	NP_001369637.1:p.Ile401Met
NM_001382709.1:c.774T>G	NP_001369638.1:p.Ile258Met
NM_001382710.1:c.1137T>G	NP_001369639.1:p.Ile379Met
NM_001382711.1:c.1185T>G	NP_001369640.1:p.Ile395Met
NM_001382712.1:c.1206T>G	NP_001369641.1:p.Ile402Met
NM_001382713.1:c.936T>G	NP_001369642.1:p.Ile312Met