Canonical Allele Identifier: CA2180427197

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58610884A= , CM000677.2:g.58610884A=	GRCh38
NC_000015.9:g.58903083A= , CM000677.1:g.58903083A=	GRCh37
NC_000015.8:g.56690375A=	NCBI36
NG_033876.1:g.144095T=
NG_033876.2:g.143824T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001110.4:c.1804+115T= MANE Select	NP_001101.1:n.1804+115T=
ENST00000260408.8:c.1804+115T= MANE Select	ENSP00000260408.3:n.1804+115T=
NM_001110.3:c.1804+115T=	NP_001101.1:n.1804+115T=
NM_001320570.1:c.1711+115T=	NP_001307499.1:n.1711+115T=
NM_001320570.2:c.1711+115T=	NP_001307499.1:n.1711+115T=
ENST00000260408.7:c.1804+115T=	ENSP00000260408.3:n.1804+115T=
ENST00000396136.6:c.1630+115T=
ENST00000402627.5:c.155-13366T=	ENSP00000386056.1:n.155-13366T=
ENST00000470269.5:n.333+115T=
ENST00000482945.5:n.1142T=
ENST00000561288.1:c.56-13366T=	ENSP00000452639.1:n.56-13366T=
XM_005254117.2:c.1711+115T=	XP_005254174.1:n.1711+115T=
XM_024449818.1:c.1582+115T=	XP_024305586.1:n.1582+115T=