Canonical Allele Identifier: CA2293866449
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547022_31547024delinsTAG , CM000680.2:g.31547022_31547024delinsTAG GRCh38
NC_000018.9:g.29126985_29126987delinsTAG , CM000680.1:g.29126985_29126987delinsTAG GRCh37
NC_000018.8:g.27380983_27380985delinsTAG NCBI36
NG_007072.3:g.53781_53783delinsTAG , LRG_397:g.53781_53783delinsTAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*279_*281delinsTAG (DSG2) MANE Select ENSP00000261590.8:n.*279_*281delinsTAG
ENST00000261590.12:c.*279_*281delinsTAG (DSG2) ENSP00000261590.8:n.*279_*281delinsTAG
NM_001943.3:c.*279_*281delinsTAG , LRG_397t1:c.*279_*281delinsTAG (DSG2) NP_001934.2:n.*279_*281delinsTAG
NR_045216.1:n.1346-1118_1346-1116delinsCTA (DSG2-AS1)
NM_001943.4:c.*279_*281delinsTAG (DSG2) NP_001934.2:n.*279_*281delinsTAG
XM_024451095.1:c.*279_*281delinsTAG (DSG2) XP_024306863.1:n.*279_*281delinsTAG
NM_001943.5:c.*279_*281delinsTAG (DSG2) MANE Select NP_001934.2:n.*279_*281delinsTAG