Canonical Allele Identifier: CA402148687
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546531A>T , CM000680.2:g.31546531A>T GRCh38
NC_000018.9:g.29126494A>T , CM000680.1:g.29126494A>T GRCh37
NC_000018.8:g.27380492A>T NCBI36
NG_007072.3:g.53290A>T , LRG_397:g.53290A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3145A>T (DSG2) MANE Select ENSP00000261590.8:p.Arg1049Ter
ENST00000261590.12:c.3145A>T (DSG2) ENSP00000261590.8:p.Arg1049Ter
NM_001943.3:c.3145A>T , LRG_397t1:c.3145A>T (DSG2) NP_001934.2:p.Arg1049Ter
NR_045216.1:n.1346-625T>A (DSG2-AS1)
NM_001943.4:c.3145A>T (DSG2) NP_001934.2:p.Arg1049Ter
XM_024451095.1:c.2611A>T (DSG2) XP_024306863.1:p.Arg871Ter
NM_001943.5:c.3145A>T (DSG2) MANE Select NP_001934.2:p.Arg1049Ter