Canonical Allele Identifier: CA1946678581

Gene: ADAM8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.133275531A= , CM000672.2:g.133275531A=	GRCh38
NC_000010.10:g.135089035A= , CM000672.1:g.135089035A=	GRCh37
NC_000010.9:g.134939025A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001109.5:c.103T= MANE Select	NP_001100.3:p.Trp35=
ENST00000445355.8:c.103T= MANE Select	ENSP00000453302.1:p.Trp35=
NM_001109.4:c.103T=	NP_001100.3:p.Trp35=
NM_001164489.1:c.103T=	NP_001157961.1:p.Trp35=
NM_001164489.2:c.103T=	NP_001157961.1:p.Trp35=
NM_001164490.1:c.46+1241T=	NP_001157962.1:n.46+1241T=
NM_001164490.2:c.46+1241T=	NP_001157962.1:n.46+1241T=
ENST00000415217.7:c.103T=	ENSP00000453855.1:p.Trp35=
ENST00000445355.7:c.103T=	ENSP00000453302.1:p.Trp35=
ENST00000463298.5:n.142T=
ENST00000485491.6:c.46+1241T=	ENSP00000453043.1:n.46+1241T=
ENST00000486609.1:c.103T=	ENSP00000453735.1:p.Trp35=
ENST00000537099.5:n.346T=
ENST00000559180.1:n.154T=
ENST00000560135.5:c.46+1241T=	ENSP00000452994.1:n.46+1241T=
XM_011539117.2:c.103T=	XP_011537419.2:p.Trp35=
XM_011539118.1:c.28T=	XP_011537420.1:p.Trp10=
XM_017015465.1:c.103T=	XP_016870954.1:p.Trp35=
XM_017015466.1:c.103T=	XP_016870955.1:p.Trp35=