Canonical Allele Identifier: CA714358806

Gene: ADAM10

Linked Data

• dbSNP Id: rs1219309210
• MyVariant Identifiers: chr15:g.58902887_58902888del (hg19) ; chr15:g.58610688_58610689del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610689_58610690del , CM000677.2:g.58610689_58610690del	GRCh38
NC_000015.9:g.58902888_58902889del , CM000677.1:g.58902888_58902889del	GRCh37
NC_000015.8:g.56690180_56690181del	NCBI36
NG_033876.1:g.144290_144291del
NG_033876.2:g.144019_144020del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.1805-172_1805-171del MANE Select	ENSP00000260408.3:n.1805-172_1805-171del
ENST00000260408.7:c.1805-172_1805-171del	ENSP00000260408.3:n.1805-172_1805-171del
ENST00000396136.6:c.1631-172_1631-171del
ENST00000402627.5:c.155-13171_155-13170del	ENSP00000386056.1:n.155-13171_155-13170del
ENST00000470269.5:n.334-172_334-171del
ENST00000482945.5:n.1337_1338del
ENST00000561288.1:c.56-13171_56-13170del	ENSP00000452639.1:n.56-13171_56-13170del
NM_001110.3:c.1805-172_1805-171del	NP_001101.1:n.1805-172_1805-171del
XM_005254117.2:c.1712-172_1712-171del	XP_005254174.1:n.1712-172_1712-171del
NM_001320570.1:c.1712-172_1712-171del	NP_001307499.1:n.1712-172_1712-171del
XM_024449818.1:c.1583-172_1583-171del	XP_024305586.1:n.1583-172_1583-171del
NM_001110.4:c.1805-172_1805-171del MANE Select	NP_001101.1:n.1805-172_1805-171del
NM_001320570.2:c.1712-172_1712-171del	NP_001307499.1:n.1712-172_1712-171del