Canonical Allele Identifier: CA2180432513

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58621372C= , CM000677.2:g.58621372C=	GRCh38
NC_000015.9:g.58913571C= , CM000677.1:g.58913571C=	GRCh37
NC_000015.8:g.56700863C=	NCBI36
NG_033876.1:g.133607G=
NG_033876.2:g.133336G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.1511+99G= MANE Select	ENSP00000260408.3:n.1511+99G=
ENST00000260408.7:c.1511+99G=	ENSP00000260408.3:n.1511+99G=
ENST00000396136.6:c.1337+99G=
ENST00000402627.5:c.154+11943G=	ENSP00000386056.1:n.154+11943G=
ENST00000462061.1:n.71+99G=
ENST00000470269.5:n.40+99G=
ENST00000475898.1:n.536+99G=
ENST00000481164.1:n.34+99G=
ENST00000482945.5:n.34+99G=
ENST00000561288.1:c.56-23854G=	ENSP00000452639.1:n.56-23854G=
NM_001110.3:c.1511+99G=	NP_001101.1:n.1511+99G=
XM_005254117.2:c.1418+99G=	XP_005254174.1:n.1418+99G=
NM_001320570.1:c.1418+99G=	NP_001307499.1:n.1418+99G=
XM_024449818.1:c.1289+99G=	XP_024305586.1:n.1289+99G=
NM_001110.4:c.1511+99G= MANE Select	NP_001101.1:n.1511+99G=
NM_001320570.2:c.1418+99G=	NP_001307499.1:n.1418+99G=