Canonical Allele Identifier: CA2180427648

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58611932C= , CM000677.2:g.58611932C=	GRCh38
NC_000015.9:g.58904131C= , CM000677.1:g.58904131C=	GRCh37
NC_000015.8:g.56691423C=	NCBI36
NG_033876.1:g.143047G=
NG_033876.2:g.142776G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001110.4:c.1571G= MANE Select	NP_001101.1:p.Cys524=
ENST00000260408.8:c.1571G= MANE Select	ENSP00000260408.3:p.Cys524=
NM_001110.3:c.1571G=	NP_001101.1:p.Cys524=
NM_001320570.1:c.1478G=	NP_001307499.1:p.Cys493=
NM_001320570.2:c.1478G=	NP_001307499.1:p.Cys493=
ENST00000260408.7:c.1571G=	ENSP00000260408.3:p.Cys524=
ENST00000396136.6:c.1397G=
ENST00000402627.5:c.155-14414G=	ENSP00000386056.1:n.155-14414G=
ENST00000462061.1:n.131G=
ENST00000470269.5:n.100G=
ENST00000475898.1:n.596G=
ENST00000481164.1:n.94G=
ENST00000482945.5:n.94G=
ENST00000561288.1:c.56-14414G=	ENSP00000452639.1:n.56-14414G=
XM_005254117.2:c.1478G=	XP_005254174.1:p.Cys493=
XM_024449818.1:c.1349G=	XP_024305586.1:p.Cys450=