Canonical Allele Identifier: CA2499216398
Gene: CD96 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111577550_111577568del , CM000665.2:g.111577550_111577568del GRCh38
NC_000003.11:g.111296397_111296415del , CM000665.1:g.111296397_111296415del GRCh37
NC_000003.10:g.112779087_112779105del NCBI36
NG_012156.1:g.40472_40490del
NG_012156.2:g.40472_40490del

Transcript Alleles

HGVS Amino-acid Change
ENST00000283285.10:c.591+1_591+19del
ENST00000352690.9:c.544-1477_544-1459del MANE Select ENSP00000342040.3:n.544-1477_544-1459del
ENST00000283285.9:c.591+1_591+19del
ENST00000352690.8:c.544-1477_544-1459del ENSP00000342040.3:n.544-1477_544-1459del
ENST00000438817.6:c.544-1477_544-1459del ENSP00000389801.2:n.544-1477_544-1459del
ENST00000465428.1:c.68-1477_68-1459del
ENST00000494798.1:c.544-1477_544-1459del ENSP00000417152.1:n.544-1477_544-1459del
NM_005816.4:c.544-1477_544-1459del NP_005807.1:n.544-1477_544-1459del
NM_198196.2:c.591+1_591+19del
XM_005247063.2:c.591+1_591+19del
XM_006713469.2:c.591+1_591+19del
XM_006713470.2:c.544-1477_544-1459del XP_006713533.1:n.544-1477_544-1459del
XR_241462.1:n.722+1_722+19del
XR_241466.1:n.675-1477_675-1459del
XR_924089.1:n.722+1_722+19del
XR_924090.1:n.722+1_722+19del
NM_001318889.1:c.544-1477_544-1459del NP_001305818.1:n.544-1477_544-1459del
NR_134917.1:n.714-1477_714-1459del
XM_005247063.3:c.591+1_591+19del
XM_006713469.3:c.591+1_591+19del
XM_006713470.3:c.544-1477_544-1459del XP_006713533.1:n.544-1477_544-1459del
XM_017005521.1:c.591+1_591+19del
XM_017005522.1:c.543+9903_543+9921del XP_016861011.1:n.543+9903_543+9921del
XR_001739977.1:n.722+1_722+19del
NM_001318889.2:c.544-1477_544-1459del NP_001305818.1:n.544-1477_544-1459del
NM_005816.5:c.544-1477_544-1459del MANE Select NP_005807.1:n.544-1477_544-1459del
NM_198196.3:c.591+1_591+19del
NR_134917.2:n.596-1477_596-1459del