Canonical Allele Identifier: CA970319593

Gene: ADAM10

Linked Data

• dbSNP Id: rs764693343
• gnomAD v3: 15-58621408-T-A
• gnomAD v4: 15-58621408-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621408T>A , CM000677.2:g.58621408T>A	GRCh38
NC_000015.9:g.58913607T>A , CM000677.1:g.58913607T>A	GRCh37
NC_000015.8:g.56700899T>A	NCBI36
NG_033876.1:g.133571A>T
NG_033876.2:g.133300A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+63A>T MANE Select	ENSP00000260408.3:n.1511+63A>T
ENST00000260408.7:c.1511+63A>T	ENSP00000260408.3:n.1511+63A>T
ENST00000396136.6:c.1337+63A>T
ENST00000402627.5:c.154+11907A>T	ENSP00000386056.1:n.154+11907A>T
ENST00000462061.1:n.71+63A>T
ENST00000470269.5:n.40+63A>T
ENST00000475898.1:n.536+63A>T
ENST00000481164.1:n.34+63A>T
ENST00000482945.5:n.34+63A>T
ENST00000561288.1:c.56-23890A>T	ENSP00000452639.1:n.56-23890A>T
NM_001110.3:c.1511+63A>T	NP_001101.1:n.1511+63A>T
XM_005254117.2:c.1418+63A>T	XP_005254174.1:n.1418+63A>T
NM_001320570.1:c.1418+63A>T	NP_001307499.1:n.1418+63A>T
XM_024449818.1:c.1289+63A>T	XP_024305586.1:n.1289+63A>T
NM_001110.4:c.1511+63A>T MANE Select	NP_001101.1:n.1511+63A>T
NM_001320570.2:c.1418+63A>T	NP_001307499.1:n.1418+63A>T