Canonical Allele Identifier: CA2180485038

Gene: ADAM10

Linked Data

• dbSNP Id: rs1899625405

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58741804_58741806del , CM000677.2:g.58741804_58741806del	GRCh38
NC_000015.9:g.59034003_59034005del , CM000677.1:g.59034003_59034005del	GRCh37
NC_000015.8:g.56821295_56821297del	NCBI36
NG_033876.1:g.13176_13178del
NG_033876.2:g.12905_12907del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.55+7677_55+7679del MANE Select	ENSP00000260408.3:n.55+7677_55+7679del
ENST00000260408.7:c.55+7677_55+7679del	ENSP00000260408.3:n.55+7677_55+7679del
ENST00000402627.5:c.55+7677_55+7679del	ENSP00000386056.1:n.55+7677_55+7679del
ENST00000439637.5:c.55+7677_55+7679del	ENSP00000391930.1:n.55+7677_55+7679del
ENST00000497846.5:n.172+6992_172+6994del
ENST00000558004.1:c.55+7677_55+7679del	ENSP00000452704.1:n.55+7677_55+7679del
ENST00000558733.5:n.291+7677_291+7679del
ENST00000559053.1:c.55+7677_55+7679del	ENSP00000453952.1:n.55+7677_55+7679del
ENST00000560608.5:n.312+7677_312+7679del
ENST00000561149.1:n.241+7677_241+7679del
ENST00000561288.1:c.55+7677_55+7679del	ENSP00000452639.1:n.55+7677_55+7679del
NM_001110.3:c.55+7677_55+7679del	NP_001101.1:n.55+7677_55+7679del
XM_005254117.2:c.55+7677_55+7679del	XP_005254174.1:n.55+7677_55+7679del
NM_001320570.1:c.55+7677_55+7679del	NP_001307499.1:n.55+7677_55+7679del
XM_024449818.1:c.-168+6992_-168+6994del	XP_024305586.1:n.-168+6992_-168+6994del
NM_001110.4:c.55+7677_55+7679del MANE Select	NP_001101.1:n.55+7677_55+7679del
NM_001320570.2:c.55+7677_55+7679del	NP_001307499.1:n.55+7677_55+7679del