Canonical Allele Identifier: CA2180427102

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610701T= , CM000677.2:g.58610701T=	GRCh38
NC_000015.9:g.58902900T= , CM000677.1:g.58902900T=	GRCh37
NC_000015.8:g.56690192T=	NCBI36
NG_033876.1:g.144278A=
NG_033876.2:g.144007A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.1805-184A= MANE Select	ENSP00000260408.3:n.1805-184A=
ENST00000260408.7:c.1805-184A=	ENSP00000260408.3:n.1805-184A=
ENST00000396136.6:c.1631-184A=
ENST00000402627.5:c.155-13183A=	ENSP00000386056.1:n.155-13183A=
ENST00000470269.5:n.334-184A=
ENST00000482945.5:n.1325A=
ENST00000561288.1:c.56-13183A=	ENSP00000452639.1:n.56-13183A=
NM_001110.3:c.1805-184A=	NP_001101.1:n.1805-184A=
XM_005254117.2:c.1712-184A=	XP_005254174.1:n.1712-184A=
NM_001320570.1:c.1712-184A=	NP_001307499.1:n.1712-184A=
XM_024449818.1:c.1583-184A=	XP_024305586.1:n.1583-184A=
NM_001110.4:c.1805-184A= MANE Select	NP_001101.1:n.1805-184A=
NM_001320570.2:c.1712-184A=	NP_001307499.1:n.1712-184A=