Canonical Allele Identifier: CA392615887

Gene: ADAM10

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1498G>T MANE Select	ENSP00000260408.3:p.Gly500Trp
ENST00000260408.7:c.1498G>T	ENSP00000260408.3:p.Gly500Trp
ENST00000396136.6:c.1324G>T
ENST00000402627.5:c.154+11831G>T	ENSP00000386056.1:n.154+11831G>T
ENST00000462061.1:n.58G>T
ENST00000470269.5:n.27G>T
ENST00000475898.1:n.523G>T
ENST00000481164.1:n.21G>T
ENST00000482945.5:n.21G>T
ENST00000561288.1:c.56-23966G>T	ENSP00000452639.1:n.56-23966G>T
NM_001110.3:c.1498G>T	NP_001101.1:p.Gly500Trp
XM_005254117.2:c.1405G>T	XP_005254174.1:p.Gly469Trp
NM_001320570.1:c.1405G>T	NP_001307499.1:p.Gly469Trp
XM_024449818.1:c.1276G>T	XP_024305586.1:p.Gly426Trp
NM_001110.4:c.1498G>T MANE Select	NP_001101.1:p.Gly500Trp
NM_001320570.2:c.1405G>T	NP_001307499.1:p.Gly469Trp