Canonical Allele Identifier: CA2180485081

Gene: ADAM10

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.58741852A= , CM000677.2:g.58741852A=	GRCh38
NC_000015.9:g.59034051A= , CM000677.1:g.59034051A=	GRCh37
NC_000015.8:g.56821343A=	NCBI36
NG_033876.1:g.13127T=
NG_033876.2:g.12856T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260408.8:c.55+7628T= MANE Select	ENSP00000260408.3:n.55+7628T=
ENST00000260408.7:c.55+7628T=	ENSP00000260408.3:n.55+7628T=
ENST00000402627.5:c.55+7628T=	ENSP00000386056.1:n.55+7628T=
ENST00000439637.5:c.55+7628T=	ENSP00000391930.1:n.55+7628T=
ENST00000497846.5:n.172+6943T=
ENST00000558004.1:c.55+7628T=	ENSP00000452704.1:n.55+7628T=
ENST00000558733.5:n.291+7628T=
ENST00000559053.1:c.55+7628T=	ENSP00000453952.1:n.55+7628T=
ENST00000560608.5:n.312+7628T=
ENST00000561149.1:n.241+7628T=
ENST00000561288.1:c.55+7628T=	ENSP00000452639.1:n.55+7628T=
NM_001110.3:c.55+7628T=	NP_001101.1:n.55+7628T=
XM_005254117.2:c.55+7628T=	XP_005254174.1:n.55+7628T=
NM_001320570.1:c.55+7628T=	NP_001307499.1:n.55+7628T=
XM_024449818.1:c.-168+6943T=	XP_024305586.1:n.-168+6943T=
NM_001110.4:c.55+7628T= MANE Select	NP_001101.1:n.55+7628T=
NM_001320570.2:c.55+7628T=	NP_001307499.1:n.55+7628T=