Canonical Allele Identifier: CA2180476239

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58665089A= , CM000677.2:g.58665089A=	GRCh38
NC_000015.9:g.58957288A= , CM000677.1:g.58957288A=	GRCh37
NC_000015.8:g.56744580A=	NCBI36
NG_033876.1:g.89890T=
NG_033876.2:g.89619T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000260408.8:c.585+8T= MANE Select	ENSP00000260408.3:n.585+8T=
ENST00000260408.7:c.585+8T=	ENSP00000260408.3:n.585+8T=
ENST00000396136.6:c.411+8T=
ENST00000402627.5:c.56-24259T=	ENSP00000386056.1:n.56-24259T=
ENST00000558733.5:n.821+8T=
ENST00000559053.1:c.56-24259T=	ENSP00000453952.1:n.56-24259T=
ENST00000561288.1:c.56-67571T=	ENSP00000452639.1:n.56-67571T=
NM_001110.3:c.585+8T=	NP_001101.1:n.585+8T=
XM_005254117.2:c.585+8T=	XP_005254174.1:n.585+8T=
NM_001320570.1:c.585+8T=	NP_001307499.1:n.585+8T=
XM_024449818.1:c.363+8T=	XP_024305586.1:n.363+8T=
NM_001110.4:c.585+8T= MANE Select	NP_001101.1:n.585+8T=
NM_001320570.2:c.585+8T=	NP_001307499.1:n.585+8T=