Canonical Allele Identifier: CA2731088546

Gene: ADAM10

Linked Data

• dbSNP Id: rs2140728690

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665067C>G , CM000677.2:g.58665067C>G	GRCh38
NC_000015.9:g.58957266C>G , CM000677.1:g.58957266C>G	GRCh37
NC_000015.8:g.56744558C>G	NCBI36
NG_033876.1:g.89912G>C
NG_033876.2:g.89641G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.585+30G>C MANE Select	ENSP00000260408.3:n.585+30G>C
ENST00000260408.7:c.585+30G>C	ENSP00000260408.3:n.585+30G>C
ENST00000396136.6:c.411+30G>C
ENST00000402627.5:c.56-24237G>C	ENSP00000386056.1:n.56-24237G>C
ENST00000558733.5:n.821+30G>C
ENST00000559053.1:c.56-24237G>C	ENSP00000453952.1:n.56-24237G>C
ENST00000561288.1:c.56-67549G>C	ENSP00000452639.1:n.56-67549G>C
NM_001110.3:c.585+30G>C	NP_001101.1:n.585+30G>C
XM_005254117.2:c.585+30G>C	XP_005254174.1:n.585+30G>C
NM_001320570.1:c.585+30G>C	NP_001307499.1:n.585+30G>C
XM_024449818.1:c.363+30G>C	XP_024305586.1:n.363+30G>C
NM_001110.4:c.585+30G>C MANE Select	NP_001101.1:n.585+30G>C
NM_001320570.2:c.585+30G>C	NP_001307499.1:n.585+30G>C