Canonical Allele Identifier: CA656962589
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546774_31546775insG , CM000680.2:g.31546774_31546775insG GRCh38
NC_000018.9:g.29126737_29126738insG , CM000680.1:g.29126737_29126738insG GRCh37
NC_000018.8:g.27380735_27380736insG NCBI36
NG_007072.3:g.53533_53534insG , LRG_397:g.53533_53534insG

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*31_*32insG (DSG2) MANE Select ENSP00000261590.8:n.*31_*32insG
ENST00000261590.12:c.*31_*32insG (DSG2) ENSP00000261590.8:n.*31_*32insG
NM_001943.3:c.*31_*32insG , LRG_397t1:c.*31_*32insG (DSG2) NP_001934.2:n.*31_*32insG
NR_045216.1:n.1346-869_1346-868insC (DSG2-AS1)
NM_001943.4:c.*31_*32insG (DSG2) NP_001934.2:n.*31_*32insG
XM_024451095.1:c.*31_*32insG (DSG2) XP_024306863.1:n.*31_*32insG
NM_001943.5:c.*31_*32insG (DSG2) MANE Select NP_001934.2:n.*31_*32insG