Canonical Allele Identifier: CA2293866226
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546522G= , CM000680.2:g.31546522G= GRCh38
NC_000018.9:g.29126485G= , CM000680.1:g.29126485G= GRCh37
NC_000018.8:g.27380483G= NCBI36
NG_007072.3:g.53281G= , LRG_397:g.53281G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.3136G= (DSG2) MANE Select ENSP00000261590.8:p.Val1046=
ENST00000261590.12:c.3136G= (DSG2) ENSP00000261590.8:p.Val1046=
NM_001943.3:c.3136G= , LRG_397t1:c.3136G= (DSG2) NP_001934.2:p.Val1046=
NR_045216.1:n.1346-616C= (DSG2-AS1)
NM_001943.4:c.3136G= (DSG2) NP_001934.2:p.Val1046=
XM_024451095.1:c.2602G= (DSG2) XP_024306863.1:p.Val868=
NM_001943.5:c.3136G= (DSG2) MANE Select NP_001934.2:p.Val1046=