Canonical Allele Identifier: CA2695227365
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546461dup , CM000680.2:g.31546461dup GRCh38
NC_000018.9:g.29126424dup , CM000680.1:g.29126424dup GRCh37
NC_000018.8:g.27380422dup NCBI36
NG_007072.3:g.53220dup , LRG_397:g.53220dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.3075dup (DSG2) MANE Select ENSP00000261590.8:p.Ser1026GlnfsTer12
ENST00000261590.12:c.3075dup (DSG2) ENSP00000261590.8:p.Ser1026GlnfsTer12
NM_001943.3:c.3075dup , LRG_397t1:c.3075dup (DSG2) NP_001934.2:p.Ser1026GlnfsTer12
NR_045216.1:n.1346-551dup (DSG2-AS1)
NM_001943.4:c.3075dup (DSG2) NP_001934.2:p.Ser1026GlnfsTer12
XM_024451095.1:c.2541dup (DSG2) XP_024306863.1:p.Ser848GlnfsTer12
NM_001943.5:c.3075dup (DSG2) MANE Select NP_001934.2:p.Ser1026GlnfsTer12