Canonical Allele Identifier: CA2180476268

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665159C= , CM000677.2:g.58665159C=	GRCh38
NC_000015.9:g.58957358C= , CM000677.1:g.58957358C=	GRCh37
NC_000015.8:g.56744650C=	NCBI36
NG_033876.1:g.89820G=
NG_033876.2:g.89549G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.523G= MANE Select	ENSP00000260408.3:p.Asp175=
ENST00000260408.7:c.523G=	ENSP00000260408.3:p.Asp175=
ENST00000396136.6:c.349G=
ENST00000402627.5:c.56-24329G=	ENSP00000386056.1:n.56-24329G=
ENST00000439637.5:c.364G=	ENSP00000391930.1:p.Asp122=
ENST00000497846.5:n.640G=
ENST00000558733.5:n.759G=
ENST00000559053.1:c.56-24329G=	ENSP00000453952.1:n.56-24329G=
ENST00000561288.1:c.56-67641G=	ENSP00000452639.1:n.56-67641G=
NM_001110.3:c.523G=	NP_001101.1:p.Asp175=
XM_005254117.2:c.523G=	XP_005254174.1:p.Asp175=
NM_001320570.1:c.523G=	NP_001307499.1:p.Asp175=
XM_024449818.1:c.301G=	XP_024305586.1:p.Asp101=
NM_001110.4:c.523G= MANE Select	NP_001101.1:p.Asp175=
NM_001320570.2:c.523G=	NP_001307499.1:p.Asp175=