Canonical Allele Identifier: CA392615885

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58621483-C-T
• COSMIC: COSM1181766
• MyVariant Identifiers: chr15:g.58913682C>T (hg19) ; chr15:g.58621483C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1499G>A MANE Select	ENSP00000260408.3:p.Gly500Glu
ENST00000260408.7:c.1499G>A	ENSP00000260408.3:p.Gly500Glu
ENST00000396136.6:c.1325G>A
ENST00000402627.5:c.154+11832G>A	ENSP00000386056.1:n.154+11832G>A
ENST00000462061.1:n.59G>A
ENST00000470269.5:n.28G>A
ENST00000475898.1:n.524G>A
ENST00000481164.1:n.22G>A
ENST00000482945.5:n.22G>A
ENST00000561288.1:c.56-23965G>A	ENSP00000452639.1:n.56-23965G>A
NM_001110.3:c.1499G>A	NP_001101.1:p.Gly500Glu
XM_005254117.2:c.1406G>A	XP_005254174.1:p.Gly469Glu
NM_001320570.1:c.1406G>A	NP_001307499.1:p.Gly469Glu
XM_024449818.1:c.1277G>A	XP_024305586.1:p.Gly426Glu
NM_001110.4:c.1499G>A MANE Select	NP_001101.1:p.Gly500Glu
NM_001320570.2:c.1406G>A	NP_001307499.1:p.Gly469Glu