Canonical Allele Identifier: CA16609309
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1198405817

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542554del , CM000680.2:g.31542554del GRCh38
NC_000018.9:g.29122517del , CM000680.1:g.29122517del GRCh37
NC_000018.8:g.27376515del NCBI36
NG_007072.3:g.49313del , LRG_397:g.49313del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2036del (DSG2) MANE Select ENSP00000261590.8:p.Gly679AlafsTer3
ENST00000261590.12:c.2036del (DSG2) ENSP00000261590.8:p.Gly679AlafsTer3
NM_001943.3:c.2036del , LRG_397t1:c.2036del (DSG2) NP_001934.2:p.Gly679AlafsTer3
NR_045216.1:n.1811-229del (DSG2-AS1)
NM_001943.4:c.2036del (DSG2) NP_001934.2:p.Gly679AlafsTer3
XM_024451095.1:c.1502del (DSG2) XP_024306863.1:p.Gly501AlafsTer3
NM_001943.5:c.2036del (DSG2) MANE Select NP_001934.2:p.Gly679AlafsTer3