Canonical Allele Identifier: CA392615886

Gene: ADAM10

Linked Data

• MyVariant Identifiers: chr15:g.58913683C>T (hg19) ; chr15:g.58621484C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621484C>T , CM000677.2:g.58621484C>T	GRCh38
NC_000015.9:g.58913683C>T , CM000677.1:g.58913683C>T	GRCh37
NC_000015.8:g.56700975C>T	NCBI36
NG_033876.1:g.133495G>A
NG_033876.2:g.133224G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1498G>A MANE Select	ENSP00000260408.3:p.Gly500Arg
ENST00000260408.7:c.1498G>A	ENSP00000260408.3:p.Gly500Arg
ENST00000396136.6:c.1324G>A
ENST00000402627.5:c.154+11831G>A	ENSP00000386056.1:n.154+11831G>A
ENST00000462061.1:n.58G>A
ENST00000470269.5:n.27G>A
ENST00000475898.1:n.523G>A
ENST00000481164.1:n.21G>A
ENST00000482945.5:n.21G>A
ENST00000561288.1:c.56-23966G>A	ENSP00000452639.1:n.56-23966G>A
NM_001110.3:c.1498G>A	NP_001101.1:p.Gly500Arg
XM_005254117.2:c.1405G>A	XP_005254174.1:p.Gly469Arg
NM_001320570.1:c.1405G>A	NP_001307499.1:p.Gly469Arg
XM_024449818.1:c.1276G>A	XP_024305586.1:p.Gly426Arg
NM_001110.4:c.1498G>A MANE Select	NP_001101.1:p.Gly500Arg
NM_001320570.2:c.1405G>A	NP_001307499.1:p.Gly469Arg