Canonical Allele Identifier: CA402142278
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31542685A>C , CM000680.2:g.31542685A>C GRCh38
NC_000018.9:g.29122648A>C , CM000680.1:g.29122648A>C GRCh37
NC_000018.8:g.27376646A>C NCBI36
NG_007072.3:g.49444A>C , LRG_397:g.49444A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2167A>C (DSG2) MANE Select ENSP00000261590.8:p.Ser723Arg
ENST00000261590.12:c.2167A>C (DSG2) ENSP00000261590.8:p.Ser723Arg
NM_001943.3:c.2167A>C , LRG_397t1:c.2167A>C (DSG2) NP_001934.2:p.Ser723Arg
NR_045216.1:n.1811-364T>G (DSG2-AS1)
NM_001943.4:c.2167A>C (DSG2) NP_001934.2:p.Ser723Arg
XM_024451095.1:c.1633A>C (DSG2) XP_024306863.1:p.Ser545Arg
NM_001943.5:c.2167A>C (DSG2) MANE Select NP_001934.2:p.Ser723Arg