Canonical Allele Identifier: CA392615883

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58621483-C-A
• MyVariant Identifiers: chr15:g.58913682C>A (hg19) ; chr15:g.58621483C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621483C>A , CM000677.2:g.58621483C>A	GRCh38
NC_000015.9:g.58913682C>A , CM000677.1:g.58913682C>A	GRCh37
NC_000015.8:g.56700974C>A	NCBI36
NG_033876.1:g.133496G>T
NG_033876.2:g.133225G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1499G>T MANE Select	ENSP00000260408.3:p.Gly500Val
ENST00000260408.7:c.1499G>T	ENSP00000260408.3:p.Gly500Val
ENST00000396136.6:c.1325G>T
ENST00000402627.5:c.154+11832G>T	ENSP00000386056.1:n.154+11832G>T
ENST00000462061.1:n.59G>T
ENST00000470269.5:n.28G>T
ENST00000475898.1:n.524G>T
ENST00000481164.1:n.22G>T
ENST00000482945.5:n.22G>T
ENST00000561288.1:c.56-23965G>T	ENSP00000452639.1:n.56-23965G>T
NM_001110.3:c.1499G>T	NP_001101.1:p.Gly500Val
XM_005254117.2:c.1406G>T	XP_005254174.1:p.Gly469Val
NM_001320570.1:c.1406G>T	NP_001307499.1:p.Gly469Val
XM_024449818.1:c.1277G>T	XP_024305586.1:p.Gly426Val
NM_001110.4:c.1499G>T MANE Select	NP_001101.1:p.Gly500Val
NM_001320570.2:c.1406G>T	NP_001307499.1:p.Gly469Val