Canonical Allele Identifier: CA2628687772

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58665055-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665055C>A , CM000677.2:g.58665055C>A	GRCh38
NC_000015.9:g.58957254C>A , CM000677.1:g.58957254C>A	GRCh37
NC_000015.8:g.56744546C>A	NCBI36
NG_033876.1:g.89924G>T
NG_033876.2:g.89653G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.585+42G>T MANE Select	ENSP00000260408.3:n.585+42G>T
ENST00000260408.7:c.585+42G>T	ENSP00000260408.3:n.585+42G>T
ENST00000396136.6:c.411+42G>T
ENST00000402627.5:c.56-24225G>T	ENSP00000386056.1:n.56-24225G>T
ENST00000558733.5:n.821+42G>T
ENST00000559053.1:c.56-24225G>T	ENSP00000453952.1:n.56-24225G>T
ENST00000561288.1:c.56-67537G>T	ENSP00000452639.1:n.56-67537G>T
NM_001110.3:c.585+42G>T	NP_001101.1:n.585+42G>T
XM_005254117.2:c.585+42G>T	XP_005254174.1:n.585+42G>T
NM_001320570.1:c.585+42G>T	NP_001307499.1:n.585+42G>T
XM_024449818.1:c.363+42G>T	XP_024305586.1:n.363+42G>T
NM_001110.4:c.585+42G>T MANE Select	NP_001101.1:n.585+42G>T
NM_001320570.2:c.585+42G>T	NP_001307499.1:n.585+42G>T