Canonical Allele Identifier: CA350695103

Gene: DES

Linked Data

• ClinVar Variation Id: 639669
• ClinVar RCV Id: RCV000792525
• dbSNP Id: rs61726467
• gnomAD v3: 2-219421553-G-T
• gnomAD v4: 2-219421553-G-T
• MyVariant Identifiers: chr2:g.220286275G>T (hg19) ; chr2:g.219421553G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219421553G>T , CM000664.2:g.219421553G>T	GRCh38
NC_000002.11:g.220286275G>T , CM000664.1:g.220286275G>T	GRCh37
NC_000002.10:g.219994519G>T	NCBI36
NG_008043.1:g.8177G>T , LRG_380:g.8177G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477226.6:n.711G>T
ENST00000683013.1:n.625G>T
ENST00000373960.4:c.1237G>T MANE Select	ENSP00000363071.3:p.Glu413Ter
ENST00000373960.3:c.1237G>T	ENSP00000363071.3:p.Glu413Ter
ENST00000477226.5:n.709G>T
ENST00000492726.1:n.632G>T
NM_001927.3:c.1237G>T , LRG_380t1:c.1237G>T	NP_001918.3:p.Glu413Ter
NM_001927.4:c.1237G>T MANE Select	NP_001918.3:p.Glu413Ter
NM_001382708.1:c.1234G>T	NP_001369637.1:p.Glu412Ter
NM_001382709.1:c.805G>T	NP_001369638.1:p.Glu269Ter
NM_001382710.1:c.1168G>T	NP_001369639.1:p.Glu390Ter
NM_001382711.1:c.1216G>T	NP_001369640.1:p.Glu406Ter
NM_001382712.1:c.1237G>T	NP_001369641.1:p.Glu413Ter
NM_001382713.1:c.967G>T	NP_001369642.1:p.Glu323Ter