Canonical Allele Identifier: CA7585497

Gene: ADAM10

Linked Data

• dbSNP Id: rs373774799
• ExAC: 15:58913675 C / A
• gnomAD v2: 15-58913675-C-A
• gnomAD v4: 15-58621476-C-A
• MyVariant Identifiers: chr15:g.58913675C>A (hg19) ; chr15:g.58621476C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621476C>A , CM000677.2:g.58621476C>A	GRCh38
NC_000015.9:g.58913675C>A , CM000677.1:g.58913675C>A	GRCh37
NC_000015.8:g.56700967C>A	NCBI36
NG_033876.1:g.133503G>T
NG_033876.2:g.133232G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1506G>T MANE Select	ENSP00000260408.3:p.Gln502His
ENST00000260408.7:c.1506G>T	ENSP00000260408.3:p.Gln502His
ENST00000396136.6:c.1332G>T
ENST00000402627.5:c.154+11839G>T	ENSP00000386056.1:n.154+11839G>T
ENST00000462061.1:n.66G>T
ENST00000470269.5:n.35G>T
ENST00000475898.1:n.531G>T
ENST00000481164.1:n.29G>T
ENST00000482945.5:n.29G>T
ENST00000561288.1:c.56-23958G>T	ENSP00000452639.1:n.56-23958G>T
NM_001110.3:c.1506G>T	NP_001101.1:p.Gln502His
XM_005254117.2:c.1413G>T	XP_005254174.1:p.Gln471His
NM_001320570.1:c.1413G>T	NP_001307499.1:p.Gln471His
XM_024449818.1:c.1284G>T	XP_024305586.1:p.Gln428His
NM_001110.4:c.1506G>T MANE Select	NP_001101.1:p.Gln502His
NM_001320570.2:c.1413G>T	NP_001307499.1:p.Gln471His