Canonical Allele Identifier: CA2293866532
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs2073319369

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547225_31547237del , CM000680.2:g.31547225_31547237del GRCh38
NC_000018.9:g.29127188_29127200del , CM000680.1:g.29127188_29127200del GRCh37
NC_000018.8:g.27381186_27381198del NCBI36
NG_007072.3:g.53984_53996del , LRG_397:g.53984_53996del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*482_*494del (DSG2) MANE Select ENSP00000261590.8:n.*482_*494del
ENST00000261590.12:c.*482_*494del (DSG2) ENSP00000261590.8:n.*482_*494del
NM_001943.3:c.*482_*494del , LRG_397t1:c.*482_*494del (DSG2) NP_001934.2:n.*482_*494del
NR_045216.1:n.1346-1329_1346-1317del (DSG2-AS1)
NM_001943.4:c.*482_*494del (DSG2) NP_001934.2:n.*482_*494del
XM_024451095.1:c.*482_*494del (DSG2) XP_024306863.1:n.*482_*494del
NM_001943.5:c.*482_*494del (DSG2) MANE Select NP_001934.2:n.*482_*494del