Canonical Allele Identifier: CA913188912
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 922976
dbSNP Id: rs2073308127

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546243del , CM000680.2:g.31546243del GRCh38
NC_000018.9:g.29126206del , CM000680.1:g.29126206del GRCh37
NC_000018.8:g.27380204del NCBI36
NG_007072.3:g.53002del , LRG_397:g.53002del

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2857del (DSG2) MANE Select ENSP00000261590.8:p.Leu953TrpfsTer11
ENST00000261590.12:c.2857del (DSG2) ENSP00000261590.8:p.Leu953TrpfsTer11
NM_001943.3:c.2857del , LRG_397t1:c.2857del (DSG2) NP_001934.2:p.Leu953TrpfsTer11
NR_045216.1:n.1346-336del (DSG2-AS1)
NM_001943.4:c.2857del (DSG2) NP_001934.2:p.Leu953TrpfsTer11
XM_024451095.1:c.2323del (DSG2) XP_024306863.1:p.Leu775TrpfsTer11
NM_001943.5:c.2857del (DSG2) MANE Select NP_001934.2:p.Leu953TrpfsTer11