Canonical Allele Identifier: CA2180476266

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665156G= , CM000677.2:g.58665156G=	GRCh38
NC_000015.9:g.58957355G= , CM000677.1:g.58957355G=	GRCh37
NC_000015.8:g.56744647G=	NCBI36
NG_033876.1:g.89823C=
NG_033876.2:g.89552C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.526C= MANE Select	ENSP00000260408.3:p.His176=
ENST00000260408.7:c.526C=	ENSP00000260408.3:p.His176=
ENST00000396136.6:c.352C=
ENST00000402627.5:c.56-24326C=	ENSP00000386056.1:n.56-24326C=
ENST00000439637.5:c.367C=	ENSP00000391930.1:p.His123=
ENST00000497846.5:n.643C=
ENST00000558733.5:n.762C=
ENST00000559053.1:c.56-24326C=	ENSP00000453952.1:n.56-24326C=
ENST00000561288.1:c.56-67638C=	ENSP00000452639.1:n.56-67638C=
NM_001110.3:c.526C=	NP_001101.1:p.His176=
XM_005254117.2:c.526C=	XP_005254174.1:p.His176=
NM_001320570.1:c.526C=	NP_001307499.1:p.His176=
XM_024449818.1:c.304C=	XP_024305586.1:p.His102=
NM_001110.4:c.526C= MANE Select	NP_001101.1:p.His176=
NM_001320570.2:c.526C=	NP_001307499.1:p.His176=