Canonical Allele Identifier: CA378825521

Gene: ADAM8

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445355.8:c.103T>A MANE Select	ENSP00000453302.1:p.Trp35Arg
ENST00000415217.7:c.103T>A	ENSP00000453855.1:p.Trp35Arg
ENST00000445355.7:c.103T>A	ENSP00000453302.1:p.Trp35Arg
ENST00000463298.5:n.142T>A
ENST00000485491.6:c.46+1241T>A	ENSP00000453043.1:n.46+1241T>A
ENST00000486609.1:c.103T>A	ENSP00000453735.1:p.Trp35Arg
ENST00000537099.5:n.346T>A
ENST00000559180.1:n.154T>A
ENST00000560135.5:c.46+1241T>A	ENSP00000452994.1:n.46+1241T>A
NM_001109.4:c.103T>A	NP_001100.3:p.Trp35Arg
NM_001164489.1:c.103T>A	NP_001157961.1:p.Trp35Arg
NM_001164490.1:c.46+1241T>A	NP_001157962.1:n.46+1241T>A
XM_011539118.1:c.28T>A	XP_011537420.1:p.Trp10Arg
XM_011539117.2:c.103T>A	XP_011537419.2:p.Trp35Arg
XM_017015465.1:c.103T>A	XP_016870954.1:p.Trp35Arg
XM_017015466.1:c.103T>A	XP_016870955.1:p.Trp35Arg
NM_001109.5:c.103T>A MANE Select	NP_001100.3:p.Trp35Arg
NM_001164489.2:c.103T>A	NP_001157961.1:p.Trp35Arg
NM_001164490.2:c.46+1241T>A	NP_001157962.1:n.46+1241T>A