Canonical Allele Identifier: CA714361057

Gene: ADAM10

Linked Data

• dbSNP Id: rs1186582718
• gnomAD v3: 15-58749908-TC-T
• gnomAD v4: 15-58749908-TC-T
• MyVariant Identifiers: chr15:g.59042108del (hg19) ; chr15:g.58749909del (hg38)

Genomic Alleles

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

Transcript Alleles

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