Canonical Allele Identifier: CA6369987
Gene: JAM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134144251G>A , CM000673.2:g.134144251G>A GRCh38
NC_000011.9:g.134014146G>A , CM000673.1:g.134014146G>A GRCh37
NC_000011.8:g.133519356G>A NCBI36
NG_028348.1:g.80327G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299106.9:c.267G>A MANE Select ENSP00000299106.4:p.Ala89=
ENST00000299106.8:c.267G>A ENSP00000299106.4:p.Ala89=
ENST00000441717.3:c.257-541G>A ENSP00000395742.3:n.257-541G>A
ENST00000524969.5:n.331G>A
ENST00000531302.5:n.266G>A
ENST00000532165.1:n.297G>A
ENST00000532252.5:c.*257G>A ENSP00000432455.1:n.*257G>A
ENST00000534549.5:c.87G>A ENSP00000433206.1:p.Ala29=
NM_001205329.1:c.257-541G>A NP_001192258.1:n.257-541G>A
NM_032801.4:c.267G>A NP_116190.3:p.Ala89=
NM_032801.5:c.267G>A MANE Select NP_116190.3:p.Ala89=
NM_001205329.2:c.257-541G>A NP_001192258.1:n.257-541G>A