Canonical Allele Identifier: CA2293866856
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547796A= , CM000680.2:g.31547796A= GRCh38
NC_000018.9:g.29127759A= , CM000680.1:g.29127759A= GRCh37
NC_000018.8:g.27381757A= NCBI36
NG_007072.3:g.54555A= , LRG_397:g.54555A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*1053A= (DSG2) MANE Select ENSP00000261590.8:n.*1053A=
ENST00000261590.12:c.*1053A= (DSG2) ENSP00000261590.8:n.*1053A=
NM_001943.3:c.*1053A= , LRG_397t1:c.*1053A= (DSG2) NP_001934.2:n.*1053A=
NR_045216.1:n.1346-1890T= (DSG2-AS1)
NM_001943.4:c.*1053A= (DSG2) NP_001934.2:n.*1053A=
NM_001943.5:c.*1053A= (DSG2) MANE Select NP_001934.2:n.*1053A=