Canonical Allele Identifier: CA2180476234

Gene: ADAM10

Linked Data

• dbSNP Id: rs1897048546

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665077G>A , CM000677.2:g.58665077G>A	GRCh38
NC_000015.9:g.58957276G>A , CM000677.1:g.58957276G>A	GRCh37
NC_000015.8:g.56744568G>A	NCBI36
NG_033876.1:g.89902C>T
NG_033876.2:g.89631C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.585+20C>T MANE Select	ENSP00000260408.3:n.585+20C>T
ENST00000260408.7:c.585+20C>T	ENSP00000260408.3:n.585+20C>T
ENST00000396136.6:c.411+20C>T
ENST00000402627.5:c.56-24247C>T	ENSP00000386056.1:n.56-24247C>T
ENST00000558733.5:n.821+20C>T
ENST00000559053.1:c.56-24247C>T	ENSP00000453952.1:n.56-24247C>T
ENST00000561288.1:c.56-67559C>T	ENSP00000452639.1:n.56-67559C>T
NM_001110.3:c.585+20C>T	NP_001101.1:n.585+20C>T
XM_005254117.2:c.585+20C>T	XP_005254174.1:n.585+20C>T
NM_001320570.1:c.585+20C>T	NP_001307499.1:n.585+20C>T
XM_024449818.1:c.363+20C>T	XP_024305586.1:n.363+20C>T
NM_001110.4:c.585+20C>T MANE Select	NP_001101.1:n.585+20C>T
NM_001320570.2:c.585+20C>T	NP_001307499.1:n.585+20C>T