Canonical Allele Identifier: CA2180432562

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621476C= , CM000677.2:g.58621476C=	GRCh38
NC_000015.9:g.58913675C= , CM000677.1:g.58913675C=	GRCh37
NC_000015.8:g.56700967C=	NCBI36
NG_033876.1:g.133503G=
NG_033876.2:g.133232G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1506G= MANE Select	ENSP00000260408.3:p.Gln502=
ENST00000260408.7:c.1506G=	ENSP00000260408.3:p.Gln502=
ENST00000396136.6:c.1332G=
ENST00000402627.5:c.154+11839G=	ENSP00000386056.1:n.154+11839G=
ENST00000462061.1:n.66G=
ENST00000470269.5:n.35G=
ENST00000475898.1:n.531G=
ENST00000481164.1:n.29G=
ENST00000482945.5:n.29G=
ENST00000561288.1:c.56-23958G=	ENSP00000452639.1:n.56-23958G=
NM_001110.3:c.1506G=	NP_001101.1:p.Gln502=
XM_005254117.2:c.1413G=	XP_005254174.1:p.Gln471=
NM_001320570.1:c.1413G=	NP_001307499.1:p.Gln471=
XM_024449818.1:c.1284G=	XP_024305586.1:p.Gln428=
NM_001110.4:c.1506G= MANE Select	NP_001101.1:p.Gln502=
NM_001320570.2:c.1413G=	NP_001307499.1:p.Gln471=