Canonical Allele Identifier: CA2293866483
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547119_31547126delinsTTTGCCTA , CM000680.2:g.31547119_31547126delinsTTTGCCTA GRCh38
NC_000018.9:g.29127082_29127089delinsTTTGCCTA , CM000680.1:g.29127082_29127089delinsTTTGCCTA GRCh37
NC_000018.8:g.27381080_27381087delinsTTTGCCTA NCBI36
NG_007072.3:g.53878_53885delinsTTTGCCTA , LRG_397:g.53878_53885delinsTTTGCCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*376_*383delinsTTTGCCTA (DSG2) MANE Select ENSP00000261590.8:n.*376_*383delinsTTTGCCTA
ENST00000261590.12:c.*376_*383delinsTTTGCCTA (DSG2) ENSP00000261590.8:n.*376_*383delinsTTTGCCTA
NM_001943.3:c.*376_*383delinsTTTGCCTA , LRG_397t1:c.*376_*383delinsTTTGCCTA (DSG2) NP_001934.2:n.*376_*383delinsTTTGCCTA
NR_045216.1:n.1346-1220_1346-1213delinsTAGGCAAA (DSG2-AS1)
NM_001943.4:c.*376_*383delinsTTTGCCTA (DSG2) NP_001934.2:n.*376_*383delinsTTTGCCTA
XM_024451095.1:c.*376_*383delinsTTTGCCTA (DSG2) XP_024306863.1:n.*376_*383delinsTTTGCCTA
NM_001943.5:c.*376_*383delinsTTTGCCTA (DSG2) MANE Select NP_001934.2:n.*376_*383delinsTTTGCCTA
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