Canonical Allele Identifier: CA383497812
Gene: JAM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.134144371T>G , CM000673.2:g.134144371T>G GRCh38
NC_000011.9:g.134014266T>G , CM000673.1:g.134014266T>G GRCh37
NC_000011.8:g.133519476T>G NCBI36
NG_028348.1:g.80447T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299106.9:c.387T>G MANE Select ENSP00000299106.4:p.Ile129Met
ENST00000299106.8:c.387T>G ENSP00000299106.4:p.Ile129Met
ENST00000441717.3:c.257-421T>G ENSP00000395742.3:n.257-421T>G
ENST00000524969.5:n.451T>G
ENST00000531302.5:n.386T>G
ENST00000532165.1:n.417T>G
ENST00000532252.5:c.*377T>G ENSP00000432455.1:n.*377T>G
ENST00000534549.5:c.207T>G ENSP00000433206.1:p.Ile69Met
NM_001205329.1:c.257-421T>G NP_001192258.1:n.257-421T>G
NM_032801.4:c.387T>G NP_116190.3:p.Ile129Met
NM_032801.5:c.387T>G MANE Select NP_116190.3:p.Ile129Met
NM_001205329.2:c.257-421T>G NP_001192258.1:n.257-421T>G