Canonical Allele Identifier: CA919958574
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1567935525

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547120_31547126del , CM000680.2:g.31547120_31547126del GRCh38
NC_000018.9:g.29127083_29127089del , CM000680.1:g.29127083_29127089del GRCh37
NC_000018.8:g.27381081_27381087del NCBI36
NG_007072.3:g.53879_53885del , LRG_397:g.53879_53885del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*377_*383del (DSG2) MANE Select ENSP00000261590.8:n.*377_*383del
ENST00000261590.12:c.*377_*383del (DSG2) ENSP00000261590.8:n.*377_*383del
NM_001943.3:c.*377_*383del , LRG_397t1:c.*377_*383del (DSG2) NP_001934.2:n.*377_*383del
NR_045216.1:n.1346-1220_1346-1214del (DSG2-AS1)
NM_001943.4:c.*377_*383del (DSG2) NP_001934.2:n.*377_*383del
XM_024451095.1:c.*377_*383del (DSG2) XP_024306863.1:n.*377_*383del
NM_001943.5:c.*377_*383del (DSG2) MANE Select NP_001934.2:n.*377_*383del