Canonical Allele Identifier: CA2293866081
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546218C= , CM000680.2:g.31546218C= GRCh38
NC_000018.9:g.29126181C= , CM000680.1:g.29126181C= GRCh37
NC_000018.8:g.27380179C= NCBI36
NG_007072.3:g.52977C= , LRG_397:g.52977C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.2832C= (DSG2) MANE Select ENSP00000261590.8:p.Ser944=
ENST00000261590.12:c.2832C= (DSG2) ENSP00000261590.8:p.Ser944=
NM_001943.3:c.2832C= , LRG_397t1:c.2832C= (DSG2) NP_001934.2:p.Ser944=
NR_045216.1:n.1346-312G= (DSG2-AS1)
NM_001943.4:c.2832C= (DSG2) NP_001934.2:p.Ser944=
XM_024451095.1:c.2298C= (DSG2) XP_024306863.1:p.Ser766=
NM_001943.5:c.2832C= (DSG2) MANE Select NP_001934.2:p.Ser944=