Canonical Allele Identifier: CA2180441892

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679182T= , CM000677.2:g.58679182T=	GRCh38
NC_000015.9:g.58971381T= , CM000677.1:g.58971381T=	GRCh37
NC_000015.8:g.56758673T=	NCBI36
NG_033876.1:g.75797A=
NG_033876.2:g.75526A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.426A= MANE Select	ENSP00000260408.3:p.Arg142=
ENST00000260408.7:c.426A=	ENSP00000260408.3:p.Arg142=
ENST00000396136.6:c.101A=
ENST00000402627.5:c.56-38352A=	ENSP00000386056.1:n.56-38352A=
ENST00000439637.5:c.325+3014A=	ENSP00000391930.1:n.325+3014A=
ENST00000497846.5:n.543A=
ENST00000558004.1:c.332-13985A=	ENSP00000452704.1:n.332-13985A=
ENST00000558733.5:n.662A=
ENST00000559053.1:c.56-38352A=	ENSP00000453952.1:n.56-38352A=
ENST00000560608.5:n.564A=
ENST00000561288.1:c.55+70298A=	ENSP00000452639.1:n.55+70298A=
NM_001110.3:c.426A=	NP_001101.1:p.Arg142=
XM_005254117.2:c.426A=	XP_005254174.1:p.Arg142=
NM_001320570.1:c.426A=	NP_001307499.1:p.Arg142=
XM_024449818.1:c.204A=	XP_024305586.1:p.Arg68=
NM_001110.4:c.426A= MANE Select	NP_001101.1:p.Arg142=
NM_001320570.2:c.426A=	NP_001307499.1:p.Arg142=