Canonical Allele Identifier: CA2628687779

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58665078-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665078C>T , CM000677.2:g.58665078C>T	GRCh38
NC_000015.9:g.58957277C>T , CM000677.1:g.58957277C>T	GRCh37
NC_000015.8:g.56744569C>T	NCBI36
NG_033876.1:g.89901G>A
NG_033876.2:g.89630G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.585+19G>A MANE Select	ENSP00000260408.3:n.585+19G>A
ENST00000260408.7:c.585+19G>A	ENSP00000260408.3:n.585+19G>A
ENST00000396136.6:c.411+19G>A
ENST00000402627.5:c.56-24248G>A	ENSP00000386056.1:n.56-24248G>A
ENST00000558733.5:n.821+19G>A
ENST00000559053.1:c.56-24248G>A	ENSP00000453952.1:n.56-24248G>A
ENST00000561288.1:c.56-67560G>A	ENSP00000452639.1:n.56-67560G>A
NM_001110.3:c.585+19G>A	NP_001101.1:n.585+19G>A
XM_005254117.2:c.585+19G>A	XP_005254174.1:n.585+19G>A
NM_001320570.1:c.585+19G>A	NP_001307499.1:n.585+19G>A
XM_024449818.1:c.363+19G>A	XP_024305586.1:n.363+19G>A
NM_001110.4:c.585+19G>A MANE Select	NP_001101.1:n.585+19G>A
NM_001320570.2:c.585+19G>A	NP_001307499.1:n.585+19G>A