Canonical Allele Identifier: CA350690245

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220284989C>A (hg19) ; chr2:g.219420267C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420267C>A , CM000664.2:g.219420267C>A	GRCh38
NC_000002.11:g.220284989C>A , CM000664.1:g.220284989C>A	GRCh37
NC_000002.10:g.219993233C>A	NCBI36
NG_008043.1:g.6891C>A , LRG_380:g.6891C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.130C>A
ENST00000683013.1:n.44C>A
ENST00000373960.4:c.656C>A MANE Select	ENSP00000363071.3:p.Thr219Asn
ENST00000373960.3:c.656C>A	ENSP00000363071.3:p.Thr219Asn
ENST00000477226.5:n.128C>A
ENST00000492726.1:n.51C>A
NM_001927.3:c.656C>A , LRG_380t1:c.656C>A	NP_001918.3:p.Thr219Asn
NM_001927.4:c.656C>A MANE Select	NP_001918.3:p.Thr219Asn
NM_001382708.1:c.653C>A	NP_001369637.1:p.Thr218Asn
NM_001382709.1:c.656C>A	NP_001369638.1:p.Thr219Asn
NM_001382710.1:c.656C>A	NP_001369639.1:p.Thr219Asn
NM_001382711.1:c.656C>A	NP_001369640.1:p.Thr219Asn
NM_001382712.1:c.656C>A	NP_001369641.1:p.Thr219Asn
NM_001382713.1:c.496-258C>A	NP_001369642.1:n.496-258C>A