Canonical Allele Identifier: CA2812004196
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31546820_31546821insT , CM000680.2:g.31546820_31546821insT GRCh38
NC_000018.9:g.29126783_29126784insT , CM000680.1:g.29126783_29126784insT GRCh37
NC_000018.8:g.27380781_27380782insT NCBI36
NG_007072.3:g.53579_53580insT , LRG_397:g.53579_53580insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*77_*78insT (DSG2) MANE Select ENSP00000261590.8:n.*77_*78insT
ENST00000261590.12:c.*77_*78insT (DSG2) ENSP00000261590.8:n.*77_*78insT
NM_001943.3:c.*77_*78insT , LRG_397t1:c.*77_*78insT (DSG2) NP_001934.2:n.*77_*78insT
NR_045216.1:n.1346-915_1346-914insA (DSG2-AS1)
NM_001943.4:c.*77_*78insT (DSG2) NP_001934.2:n.*77_*78insT
XM_024451095.1:c.*77_*78insT (DSG2) XP_024306863.1:n.*77_*78insT
NM_001943.5:c.*77_*78insT (DSG2) MANE Select NP_001934.2:n.*77_*78insT