Canonical Allele Identifier: CA778425894
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1424201257

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546839_31546840del , CM000680.2:g.31546839_31546840del GRCh38
NC_000018.9:g.29126802_29126803del , CM000680.1:g.29126802_29126803del GRCh37
NC_000018.8:g.27380800_27380801del NCBI36
NG_007072.3:g.53598_53599del , LRG_397:g.53598_53599del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*96_*97del (DSG2) MANE Select ENSP00000261590.8:n.*96_*97del
ENST00000261590.12:c.*96_*97del (DSG2) ENSP00000261590.8:n.*96_*97del
NM_001943.3:c.*96_*97del , LRG_397t1:c.*96_*97del (DSG2) NP_001934.2:n.*96_*97del
NR_045216.1:n.1346-929_1346-928del (DSG2-AS1)
NM_001943.4:c.*96_*97del (DSG2) NP_001934.2:n.*96_*97del
XM_024451095.1:c.*96_*97del (DSG2) XP_024306863.1:n.*96_*97del
NM_001943.5:c.*96_*97del (DSG2) MANE Select NP_001934.2:n.*96_*97del