Canonical Allele Identifier: CA970326843
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1899931000

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749927del , CM000677.2:g.58749927del GRCh38
NC_000015.9:g.59042126del , CM000677.1:g.59042126del GRCh37
NC_000015.8:g.56829418del NCBI36
NG_033876.1:g.5055del
NG_033876.2:g.4784del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-390del ENSP00000260408.3:n.-390del
NM_001110.3:c.-390del NP_001101.1:n.-390del
NM_001320570.1:c.-390del NP_001307499.1:n.-390del