Canonical Allele Identifier: CA2628685309

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58610687-T-G

Genomic Alleles

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

Transcript Alleles

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