Canonical Allele Identifier: CA2506904799
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546887_31546888del , CM000680.2:g.31546887_31546888del GRCh38
NC_000018.9:g.29126850_29126851del , CM000680.1:g.29126850_29126851del GRCh37
NC_000018.8:g.27380848_27380849del NCBI36
NG_007072.3:g.53646_53647del , LRG_397:g.53646_53647del

Transcript Alleles

HGVS Amino-acid change
ENST00000261590.13:c.*144_*145del (DSG2) MANE Select ENSP00000261590.8:n.*144_*145del
ENST00000261590.12:c.*144_*145del (DSG2) ENSP00000261590.8:n.*144_*145del
NM_001943.3:c.*144_*145del , LRG_397t1:c.*144_*145del (DSG2) NP_001934.2:n.*144_*145del
NR_045216.1:n.1346-982_1346-981del (DSG2-AS1)
NM_001943.4:c.*144_*145del (DSG2) NP_001934.2:n.*144_*145del
XM_024451095.1:c.*144_*145del (DSG2) XP_024306863.1:n.*144_*145del
NM_001943.5:c.*144_*145del (DSG2) MANE Select NP_001934.2:n.*144_*145del