Canonical Allele Identifier: CA490493720

Gene: ADAM10

Linked Data

• gnomAD v4: 15-58621482-C-T
• MyVariant Identifiers: chr15:g.58913681C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621482C>T , CM000677.2:g.58621482C>T	GRCh38
NC_000015.9:g.58913681C>T , CM000677.1:g.58913681C>T	GRCh37
NC_000015.8:g.56700973C>T	NCBI36
NG_033876.1:g.133497G>A
NG_033876.2:g.133226G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1500G>A MANE Select	ENSP00000260408.3:p.Gly500=
ENST00000260408.7:c.1500G>A	ENSP00000260408.3:p.Gly500=
ENST00000396136.6:c.1326G>A
ENST00000402627.5:c.154+11833G>A	ENSP00000386056.1:n.154+11833G>A
ENST00000462061.1:n.60G>A
ENST00000470269.5:n.29G>A
ENST00000475898.1:n.525G>A
ENST00000481164.1:n.23G>A
ENST00000482945.5:n.23G>A
ENST00000561288.1:c.56-23964G>A	ENSP00000452639.1:n.56-23964G>A
NM_001110.3:c.1500G>A	NP_001101.1:p.Gly500=
XM_005254117.2:c.1407G>A	XP_005254174.1:p.Gly469=
NM_001320570.1:c.1407G>A	NP_001307499.1:p.Gly469=
XM_024449818.1:c.1278G>A	XP_024305586.1:p.Gly426=
NM_001110.4:c.1500G>A MANE Select	NP_001101.1:p.Gly500=
NM_001320570.2:c.1407G>A	NP_001307499.1:p.Gly469=