Canonical Allele Identifier: CA2293866182
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546407T= , CM000680.2:g.31546407T= GRCh38
NC_000018.9:g.29126370T= , CM000680.1:g.29126370T= GRCh37
NC_000018.8:g.27380368T= NCBI36
NG_007072.3:g.53166T= , LRG_397:g.53166T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3021T= (DSG2) MANE Select ENSP00000261590.8:p.His1007=
ENST00000261590.12:c.3021T= (DSG2) ENSP00000261590.8:p.His1007=
NM_001943.3:c.3021T= , LRG_397t1:c.3021T= (DSG2) NP_001934.2:p.His1007=
NR_045216.1:n.1346-501A= (DSG2-AS1)
NM_001943.4:c.3021T= (DSG2) NP_001934.2:p.His1007=
XM_024451095.1:c.2487T= (DSG2) XP_024306863.1:p.His829=
NM_001943.5:c.3021T= (DSG2) MANE Select NP_001934.2:p.His1007=