Canonical Allele Identifier: CA2293766650
Gene: DSG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31326550A= , CM000680.2:g.31326550A= GRCh38
NC_000018.9:g.28906513A= , CM000680.1:g.28906513A= GRCh37
NC_000018.8:g.27160511A= NCBI36
NG_011803.2:g.13462A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257192.5:c.49-31A= MANE Select ENSP00000257192.4:n.49-31A=
ENST00000257192.4:c.49-31A= ENSP00000257192.4:n.49-31A=
NM_001942.3:c.49-31A= NP_001933.2:n.49-31A=
NM_001942.4:c.49-31A= MANE Select NP_001933.2:n.49-31A=
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