Canonical Allele Identifier: CA2180493062
Gene: ADAM10 HGNC NCBI

Linked Data

dbSNP Id: rs1567024479

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.58749893_58749905del , CM000677.2:g.58749893_58749905del GRCh38
NC_000015.9:g.59042092_59042104del , CM000677.1:g.59042092_59042104del GRCh37
NC_000015.8:g.56829384_56829396del NCBI36
NG_033876.1:g.5084_5096del
NG_033876.2:g.4813_4825del

Transcript Alleles

HGVS Amino-acid Change
ENST00000260408.7:c.-361_-349del ENSP00000260408.3:n.-361_-349del
NM_001110.3:c.-361_-349del NP_001101.1:n.-361_-349del
NM_001320570.1:c.-361_-349del NP_001307499.1:n.-361_-349del