Canonical Allele Identifier: CA2293866701
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547536G= , CM000680.2:g.31547536G= GRCh38
NC_000018.9:g.29127499G= , CM000680.1:g.29127499G= GRCh37
NC_000018.8:g.27381497G= NCBI36
NG_007072.3:g.54295G= , LRG_397:g.54295G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*793G= (DSG2) MANE Select ENSP00000261590.8:n.*793G=
ENST00000261590.12:c.*793G= (DSG2) ENSP00000261590.8:n.*793G=
NM_001943.3:c.*793G= , LRG_397t1:c.*793G= (DSG2) NP_001934.2:n.*793G=
NR_045216.1:n.1346-1630C= (DSG2-AS1)
NM_001943.4:c.*793G= (DSG2) NP_001934.2:n.*793G=
NM_001943.5:c.*793G= (DSG2) MANE Select NP_001934.2:n.*793G=