Canonical Allele Identifier: CA2293866542
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547244_31547250delinsATAACTT , CM000680.2:g.31547244_31547250delinsATAACTT GRCh38
NC_000018.9:g.29127207_29127213delinsATAACTT , CM000680.1:g.29127207_29127213delinsATAACTT GRCh37
NC_000018.8:g.27381205_27381211delinsATAACTT NCBI36
NG_007072.3:g.54003_54009delinsATAACTT , LRG_397:g.54003_54009delinsATAACTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*501_*507delinsATAACTT (DSG2) MANE Select ENSP00000261590.8:n.*501_*507delinsATAACTT
ENST00000261590.12:c.*501_*507delinsATAACTT (DSG2) ENSP00000261590.8:n.*501_*507delinsATAACTT
NM_001943.3:c.*501_*507delinsATAACTT , LRG_397t1:c.*501_*507delinsATAACTT (DSG2) NP_001934.2:n.*501_*507delinsATAACTT
NR_045216.1:n.1346-1344_1346-1338delinsAAGTTAT (DSG2-AS1)
NM_001943.4:c.*501_*507delinsATAACTT (DSG2) NP_001934.2:n.*501_*507delinsATAACTT
XM_024451095.1:c.*501_*507delinsATAACTT (DSG2) XP_024306863.1:n.*501_*507delinsATAACTT
NM_001943.5:c.*501_*507delinsATAACTT (DSG2) MANE Select NP_001934.2:n.*501_*507delinsATAACTT