Canonical Allele Identifier: CA350690184

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220284980A>T (hg19) ; chr2:g.219420258A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219420258A>T , CM000664.2:g.219420258A>T	GRCh38
NC_000002.11:g.220284980A>T , CM000664.1:g.220284980A>T	GRCh37
NC_000002.10:g.219993224A>T	NCBI36
NG_008043.1:g.6882A>T , LRG_380:g.6882A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000477226.6:n.121A>T
ENST00000683013.1:n.35A>T
ENST00000373960.4:c.647A>T MANE Select	ENSP00000363071.3:p.Asp216Val
ENST00000373960.3:c.647A>T	ENSP00000363071.3:p.Asp216Val
ENST00000477226.5:n.119A>T
ENST00000492726.1:n.42A>T
NM_001927.3:c.647A>T , LRG_380t1:c.647A>T	NP_001918.3:p.Asp216Val
NM_001927.4:c.647A>T MANE Select	NP_001918.3:p.Asp216Val
NM_001382708.1:c.644A>T	NP_001369637.1:p.Asp215Val
NM_001382709.1:c.647A>T	NP_001369638.1:p.Asp216Val
NM_001382710.1:c.647A>T	NP_001369639.1:p.Asp216Val
NM_001382711.1:c.647A>T	NP_001369640.1:p.Asp216Val
NM_001382712.1:c.647A>T	NP_001369641.1:p.Asp216Val
NM_001382713.1:c.496-267A>T	NP_001369642.1:n.496-267A>T