Canonical Allele Identifier: CA970326788

Gene: ADAM10

Linked Data

• dbSNP Id: rs1899928462
• gnomAD v3: 15-58749880-C-CCGCGCCCCTACCT
• gnomAD v4: 15-58749880-C-CCGCGCCCCTACCT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58749882_58749894dup , CM000677.2:g.58749882_58749894dup	GRCh38
NC_000015.9:g.59042081_59042093dup , CM000677.1:g.59042081_59042093dup	GRCh37
NC_000015.8:g.56829373_56829385dup	NCBI36
NG_033876.1:g.5086_5098dup
NG_033876.2:g.4815_4827dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.7:c.-359_-347dup	ENSP00000260408.3:n.-359_-347dup
NM_001110.3:c.-359_-347dup	NP_001101.1:n.-359_-347dup
NM_001320570.1:c.-359_-347dup	NP_001307499.1:n.-359_-347dup