Canonical Allele Identifier: CA778425908
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1177090586

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546874_31546875del , CM000680.2:g.31546874_31546875del GRCh38
NC_000018.9:g.29126837_29126838del , CM000680.1:g.29126837_29126838del GRCh37
NC_000018.8:g.27380835_27380836del NCBI36
NG_007072.3:g.53633_53634del , LRG_397:g.53633_53634del

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*131_*132del (DSG2) MANE Select ENSP00000261590.8:n.*131_*132del
ENST00000261590.12:c.*131_*132del (DSG2) ENSP00000261590.8:n.*131_*132del
NM_001943.3:c.*131_*132del , LRG_397t1:c.*131_*132del (DSG2) NP_001934.2:n.*131_*132del
NR_045216.1:n.1346-969_1346-968del (DSG2-AS1)
NM_001943.4:c.*131_*132del (DSG2) NP_001934.2:n.*131_*132del
XM_024451095.1:c.*131_*132del (DSG2) XP_024306863.1:n.*131_*132del
NM_001943.5:c.*131_*132del (DSG2) MANE Select NP_001934.2:n.*131_*132del