Canonical Allele Identifier: CA2580616703
Gene: DES HGNC NCBI

Linked Data

ClinVar Variation Id: 2091637
ClinVar RCV Id: RCV003015700

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219418987_219418988dup , CM000664.2:g.219418987_219418988dup GRCh38
NC_000002.11:g.220283709_220283710dup , CM000664.1:g.220283709_220283710dup GRCh37
NC_000002.10:g.219991953_219991954dup NCBI36
NG_008043.1:g.5611_5612dup , LRG_380:g.5611_5612dup

Transcript Alleles

HGVS Amino-acid change
ENST00000373960.4:c.525_526dup MANE Select ENSP00000363071.3:p.Val176AlafsTer26
ENST00000373960.3:c.525_526dup ENSP00000363071.3:p.Val176AlafsTer26
NM_001927.3:c.525_526dup , LRG_380t1:c.525_526dup NP_001918.3:p.Val176AlafsTer26
NM_001927.4:c.525_526dup MANE Select NP_001918.3:p.Val176AlafsTer26
NM_001382708.1:c.525_526dup NP_001369637.1:p.Val176AlafsTer26
NM_001382709.1:c.525_526dup NP_001369638.1:p.Val176AlafsTer26
NM_001382710.1:c.525_526dup NP_001369639.1:p.Val176AlafsTer26
NM_001382711.1:c.525_526dup NP_001369640.1:p.Val176AlafsTer26
NM_001382712.1:c.525_526dup NP_001369641.1:p.Val176AlafsTer26
NM_001382713.1:c.495+30_495+31dup NP_001369642.1:n.495+30_495+31dup