Canonical Allele Identifier: CA2293866533
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547223T= , CM000680.2:g.31547223T= GRCh38
NC_000018.9:g.29127186T= , CM000680.1:g.29127186T= GRCh37
NC_000018.8:g.27381184T= NCBI36
NG_007072.3:g.53982T= , LRG_397:g.53982T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*480T= (DSG2) MANE Select ENSP00000261590.8:n.*480T=
ENST00000261590.12:c.*480T= (DSG2) ENSP00000261590.8:n.*480T=
NM_001943.3:c.*480T= , LRG_397t1:c.*480T= (DSG2) NP_001934.2:n.*480T=
NR_045216.1:n.1346-1317A= (DSG2-AS1)
NM_001943.4:c.*480T= (DSG2) NP_001934.2:n.*480T=
XM_024451095.1:c.*480T= (DSG2) XP_024306863.1:n.*480T=
NM_001943.5:c.*480T= (DSG2) MANE Select NP_001934.2:n.*480T=