Canonical Allele Identifier: CA350695112

Gene: DES

Linked Data

• MyVariant Identifiers: chr2:g.220286277G>T (hg19) ; chr2:g.219421555G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421555G>T , CM000664.2:g.219421555G>T	GRCh38
NC_000002.11:g.220286277G>T , CM000664.1:g.220286277G>T	GRCh37
NC_000002.10:g.219994521G>T	NCBI36
NG_008043.1:g.8179G>T , LRG_380:g.8179G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.713G>T
ENST00000683013.1:n.627G>T
ENST00000373960.4:c.1239G>T MANE Select	ENSP00000363071.3:p.Glu413Asp
ENST00000373960.3:c.1239G>T	ENSP00000363071.3:p.Glu413Asp
ENST00000477226.5:n.711G>T
ENST00000492726.1:n.634G>T
NM_001927.3:c.1239G>T , LRG_380t1:c.1239G>T	NP_001918.3:p.Glu413Asp
NM_001927.4:c.1239G>T MANE Select	NP_001918.3:p.Glu413Asp
NM_001382708.1:c.1236G>T	NP_001369637.1:p.Glu412Asp
NM_001382709.1:c.807G>T	NP_001369638.1:p.Glu269Asp
NM_001382710.1:c.1170G>T	NP_001369639.1:p.Glu390Asp
NM_001382711.1:c.1218G>T	NP_001369640.1:p.Glu406Asp
NM_001382712.1:c.1239G>T	NP_001369641.1:p.Glu413Asp
NM_001382713.1:c.969G>T	NP_001369642.1:p.Glu323Asp