Canonical Allele Identifier: CA2180441897

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58679193G= , CM000677.2:g.58679193G=	GRCh38
NC_000015.9:g.58971392G= , CM000677.1:g.58971392G=	GRCh37
NC_000015.8:g.56758684G=	NCBI36
NG_033876.1:g.75786C=
NG_033876.2:g.75515C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001110.4:c.415C= MANE Select	NP_001101.1:p.Pro139=
ENST00000260408.8:c.415C= MANE Select	ENSP00000260408.3:p.Pro139=
NM_001110.3:c.415C=	NP_001101.1:p.Pro139=
NM_001320570.1:c.415C=	NP_001307499.1:p.Pro139=
NM_001320570.2:c.415C=	NP_001307499.1:p.Pro139=
ENST00000260408.7:c.415C=	ENSP00000260408.3:p.Pro139=
ENST00000396136.6:c.90C=
ENST00000402627.5:c.56-38363C=	ENSP00000386056.1:n.56-38363C=
ENST00000439637.5:c.325+3003C=	ENSP00000391930.1:n.325+3003C=
ENST00000497846.5:n.532C=
ENST00000558004.1:c.332-13996C=	ENSP00000452704.1:n.332-13996C=
ENST00000558733.5:n.651C=
ENST00000559053.1:c.56-38363C=	ENSP00000453952.1:n.56-38363C=
ENST00000560608.5:n.553C=
ENST00000561288.1:c.55+70287C=	ENSP00000452639.1:n.55+70287C=
XM_005254117.2:c.415C=	XP_005254174.1:p.Pro139=
XM_024449818.1:c.193C=	XP_024305586.1:p.Pro65=