Canonical Allele Identifier: CA021775
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs794728098

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31545758_31545759del , CM000680.2:g.31545758_31545759del GRCh38
NC_000018.9:g.29125721_29125722del , CM000680.1:g.29125721_29125722del GRCh37
NC_000018.8:g.27379719_27379720del NCBI36
NG_007072.3:g.52517_52518del , LRG_397:g.52517_52518del

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.2372_2373del (DSG2) MANE Select ENSP00000261590.8:p.Thr791SerfsTer14
ENST00000261590.12:c.2372_2373del (DSG2) ENSP00000261590.8:p.Thr791SerfsTer14
NM_001943.3:c.2372_2373del , LRG_397t1:c.2372_2373del (DSG2) NP_001934.2:p.Thr791SerfsTer14
NR_045216.1:n.1497_1498del (DSG2-AS1)
NM_001943.4:c.2372_2373del (DSG2) NP_001934.2:p.Thr791SerfsTer14
XM_024451095.1:c.1838_1839del (DSG2) XP_024306863.1:p.Thr613SerfsTer14
NM_001943.5:c.2372_2373del (DSG2) MANE Select NP_001934.2:p.Thr791SerfsTer14