Canonical Allele Identifier: CA402127451
Gene: DSG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.28906567A>C (hg19) chr18:g.31326604A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31326604A>C , CM000680.2:g.31326604A>C GRCh38
NC_000018.9:g.28906567A>C , CM000680.1:g.28906567A>C GRCh37
NC_000018.8:g.27160565A>C NCBI36
NG_011803.2:g.13516A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000257192.5:c.72A>C MANE Select ENSP00000257192.4:p.Glu24Asp
ENST00000257192.4:c.72A>C ENSP00000257192.4:p.Glu24Asp
NM_001942.3:c.72A>C NP_001933.2:p.Glu24Asp
NM_001942.4:c.72A>C MANE Select NP_001933.2:p.Glu24Asp
Search 100 bp 5'
Search 100 bp 3'