Canonical Allele Identifier: CA2293766661
Gene: DSG1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31326571T= , CM000680.2:g.31326571T= GRCh38
NC_000018.9:g.28906534T= , CM000680.1:g.28906534T= GRCh37
NC_000018.8:g.27160532T= NCBI36
NG_011803.2:g.13483T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000257192.5:c.49-10T= MANE Select ENSP00000257192.4:n.49-10T=
ENST00000257192.4:c.49-10T= ENSP00000257192.4:n.49-10T=
NM_001942.3:c.49-10T= NP_001933.2:n.49-10T=
NM_001942.4:c.49-10T= MANE Select NP_001933.2:n.49-10T=