Canonical Allele Identifier: CA2293866851
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547791G= , CM000680.2:g.31547791G= GRCh38
NC_000018.9:g.29127754G= , CM000680.1:g.29127754G= GRCh37
NC_000018.8:g.27381752G= NCBI36
NG_007072.3:g.54550G= , LRG_397:g.54550G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*1048G= (DSG2) MANE Select ENSP00000261590.8:n.*1048G=
ENST00000261590.12:c.*1048G= (DSG2) ENSP00000261590.8:n.*1048G=
NM_001943.3:c.*1048G= , LRG_397t1:c.*1048G= (DSG2) NP_001934.2:n.*1048G=
NR_045216.1:n.1346-1885C= (DSG2-AS1)
NM_001943.4:c.*1048G= (DSG2) NP_001934.2:n.*1048G=
NM_001943.5:c.*1048G= (DSG2) MANE Select NP_001934.2:n.*1048G=