Canonical Allele Identifier: CA2293866561
Gene: DSG2 HGNC NCBI
DSG2-AS1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31547275_31547277delinsCTG , CM000680.2:g.31547275_31547277delinsCTG GRCh38
NC_000018.9:g.29127238_29127240delinsCTG , CM000680.1:g.29127238_29127240delinsCTG GRCh37
NC_000018.8:g.27381236_27381238delinsCTG NCBI36
NG_007072.3:g.54034_54036delinsCTG , LRG_397:g.54034_54036delinsCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000261590.13:c.*532_*534delinsCTG (DSG2) MANE Select ENSP00000261590.8:n.*532_*534delinsCTG
ENST00000261590.12:c.*532_*534delinsCTG (DSG2) ENSP00000261590.8:n.*532_*534delinsCTG
NM_001943.3:c.*532_*534delinsCTG , LRG_397t1:c.*532_*534delinsCTG (DSG2) NP_001934.2:n.*532_*534delinsCTG
NR_045216.1:n.1346-1371_1346-1369delinsCAG (DSG2-AS1)
NM_001943.4:c.*532_*534delinsCTG (DSG2) NP_001934.2:n.*532_*534delinsCTG
XM_024451095.1:c.*532_*534delinsCTG (DSG2) XP_024306863.1:n.*532_*534delinsCTG
NM_001943.5:c.*532_*534delinsCTG (DSG2) MANE Select NP_001934.2:n.*532_*534delinsCTG
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