Canonical Allele Identifier: CA431427803

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220285225T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420503T>G , CM000664.2:g.219420503T>G	GRCh38
NC_000002.11:g.220285225T>G , CM000664.1:g.220285225T>G	GRCh37
NC_000002.10:g.219993469T>G	NCBI36
NG_008043.1:g.7127T>G , LRG_380:g.7127T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.218T>G
ENST00000683013.1:n.132T>G
ENST00000373960.4:c.744T>G MANE Select	ENSP00000363071.3:p.Arg248=
ENST00000373960.3:c.744T>G	ENSP00000363071.3:p.Arg248=
ENST00000477226.5:n.216T>G
ENST00000492726.1:n.139T>G
NM_001927.3:c.744T>G , LRG_380t1:c.744T>G	NP_001918.3:p.Arg248=
NM_001927.4:c.744T>G MANE Select	NP_001918.3:p.Arg248=
NM_001382708.1:c.741T>G	NP_001369637.1:p.Arg247=
NM_001382709.1:c.735+157T>G	NP_001369638.1:n.735+157T>G
NM_001382710.1:c.744T>G	NP_001369639.1:p.Arg248=
NM_001382711.1:c.744T>G	NP_001369640.1:p.Arg248=
NM_001382712.1:c.744T>G	NP_001369641.1:p.Arg248=
NM_001382713.1:c.496-22T>G	NP_001369642.1:n.496-22T>G