Canonical Allele Identifier: CA2293859918
Gene: DSG2 HGNC NCBI

Linked Data

dbSNP Id: rs2073198276

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31531435del , CM000680.2:g.31531435del GRCh38
NC_000018.9:g.29111398del , CM000680.1:g.29111398del GRCh37
NC_000018.8:g.27365396del NCBI36
NG_007072.3:g.38194del , LRG_397:g.38194del

Transcript Alleles

HGVS Amino-acid Change
ENST00000683614.2:n.1294del
ENST00000683614.1:c.1294del
ENST00000261590.13:c.1280+183del MANE Select ENSP00000261590.8:n.1280+183del
ENST00000261590.12:c.1280+183del ENSP00000261590.8:n.1280+183del
NM_001943.3:c.1280+183del , LRG_397t1:c.1280+183del NP_001934.2:n.1280+183del
NM_001943.4:c.1280+183del NP_001934.2:n.1280+183del
XM_024451095.1:c.746+183del XP_024306863.1:n.746+183del
NM_001943.5:c.1280+183del MANE Select NP_001934.2:n.1280+183del