Canonical Allele Identifier: CA490492327

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665172C>T , CM000677.2:g.58665172C>T	GRCh38
NC_000015.9:g.58957371C>T , CM000677.1:g.58957371C>T	GRCh37
NC_000015.8:g.56744663C>T	NCBI36
NG_033876.1:g.89807G>A
NG_033876.2:g.89536G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110.4:c.510G>A MANE Select	NP_001101.1:p.Gln170=
ENST00000260408.8:c.510G>A MANE Select	ENSP00000260408.3:p.Gln170=
NM_001110.3:c.510G>A	NP_001101.1:p.Gln170=
NM_001320570.1:c.510G>A	NP_001307499.1:p.Gln170=
NM_001320570.2:c.510G>A	NP_001307499.1:p.Gln170=
ENST00000260408.7:c.510G>A	ENSP00000260408.3:p.Gln170=
ENST00000396136.6:c.336G>A
ENST00000402627.5:c.56-24342G>A	ENSP00000386056.1:n.56-24342G>A
ENST00000439637.5:c.351G>A	ENSP00000391930.1:p.Gln117=
ENST00000497846.5:n.627G>A
ENST00000558733.5:n.746G>A
ENST00000559053.1:c.56-24342G>A	ENSP00000453952.1:n.56-24342G>A
ENST00000561288.1:c.56-67654G>A	ENSP00000452639.1:n.56-67654G>A
XM_005254117.2:c.510G>A	XP_005254174.1:p.Gln170=
XM_024449818.1:c.288G>A	XP_024305586.1:p.Gln96=