Canonical Allele Identifier: CA714361051

Gene: ADAM10

Linked Data

• dbSNP Id: rs1186582718
• gnomAD v3: 15-58749908-T-TC
• gnomAD v4: 15-58749908-T-TC
• MyVariant Identifiers: chr15:g.59042107_59042108insC (hg19) ; chr15:g.58749908_58749909insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58749913dup , CM000677.2:g.58749913dup	GRCh38
NC_000015.9:g.59042112dup , CM000677.1:g.59042112dup	GRCh37
NC_000015.8:g.56829404dup	NCBI36
NG_033876.1:g.5070dup
NG_033876.2:g.4799dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.7:c.-375dup	ENSP00000260408.3:n.-375dup
NM_001110.3:c.-375dup	NP_001101.1:n.-375dup
NM_001320570.1:c.-375dup	NP_001307499.1:n.-375dup