Canonical Allele Identifier: CA2580068573

Gene: CD96

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111638185A>G , CM000665.2:g.111638185A>G	GRCh38
NC_000003.11:g.111357032A>G , CM000665.1:g.111357032A>G	GRCh37
NC_000003.10:g.112839722A>G	NCBI36
NG_012156.1:g.101107A>G
NG_012156.2:g.101107A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005816.5:c.1477+17A>G MANE Select	NP_005807.1:n.1477+17A>G
ENST00000352690.9:c.1477+17A>G MANE Select	ENSP00000342040.3:n.1477+17A>G
NM_005816.4:c.1477+17A>G	NP_005807.1:n.1477+17A>G
NM_198196.2:c.1525+17A>G	NP_937839.1:n.1525+17A>G
NM_198196.3:c.1525+17A>G	NP_937839.1:n.1525+17A>G
NR_134917.1:n.1644+17A>G
NR_134917.2:n.1526+17A>G
ENST00000283285.10:c.1525+17A>G	ENSP00000283285.5:n.1525+17A>G
ENST00000283285.9:c.1525+17A>G	ENSP00000283285.5:n.1525+17A>G
ENST00000352690.8:c.1477+17A>G	ENSP00000342040.3:n.1477+17A>G
ENST00000494798.1:c.1474+17A>G	ENSP00000417152.1:n.1474+17A>G
XM_006713469.2:c.1522+17A>G	XP_006713532.1:n.1522+17A>G
XM_006713469.3:c.1522+17A>G	XP_006713532.1:n.1522+17A>G
XM_006713470.2:c.1474+17A>G	XP_006713533.1:n.1474+17A>G
XM_006713470.3:c.1474+17A>G	XP_006713533.1:n.1474+17A>G
XM_011512324.1:c.742+17A>G	XP_011510626.1:n.742+17A>G
XM_017005521.1:c.1336+17A>G	XP_016861010.1:n.1336+17A>G
XM_017005522.1:c.1213+17A>G	XP_016861011.1:n.1213+17A>G
XR_001739977.1:n.1656+17A>G
XR_241462.1:n.1656+17A>G
XR_241466.1:n.1605+17A>G
XR_924089.1:n.1656+17A>G
XR_924090.1:n.1656+17A>G