Canonical Allele Identifier: CA2628685308

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58610687-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610687T>C , CM000677.2:g.58610687T>C	GRCh38
NC_000015.9:g.58902886T>C , CM000677.1:g.58902886T>C	GRCh37
NC_000015.8:g.56690178T>C	NCBI36
NG_033876.1:g.144292A>G
NG_033876.2:g.144021A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.1805-170A>G MANE Select	ENSP00000260408.3:n.1805-170A>G
ENST00000260408.7:c.1805-170A>G	ENSP00000260408.3:n.1805-170A>G
ENST00000396136.6:c.1631-170A>G
ENST00000402627.5:c.155-13169A>G	ENSP00000386056.1:n.155-13169A>G
ENST00000470269.5:n.334-170A>G
ENST00000482945.5:n.1339A>G
ENST00000561288.1:c.56-13169A>G	ENSP00000452639.1:n.56-13169A>G
NM_001110.3:c.1805-170A>G	NP_001101.1:n.1805-170A>G
XM_005254117.2:c.1712-170A>G	XP_005254174.1:n.1712-170A>G
NM_001320570.1:c.1712-170A>G	NP_001307499.1:n.1712-170A>G
XM_024449818.1:c.1583-170A>G	XP_024305586.1:n.1583-170A>G
NM_001110.4:c.1805-170A>G MANE Select	NP_001101.1:n.1805-170A>G
NM_001320570.2:c.1712-170A>G	NP_001307499.1:n.1712-170A>G