Canonical Allele Identifier: CA1393487122

Gene: CD96

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.111585362C= , CM000665.2:g.111585362C=	GRCh38
NC_000003.11:g.111304209C= , CM000665.1:g.111304209C=	GRCh37
NC_000003.10:g.112786899C=	NCBI36
NG_012156.1:g.48284C=
NG_012156.2:g.48284C=

Transcript Alleles

HGVS	Amino-acid Change
NM_005816.5:c.791C= MANE Select	NP_005807.1:p.Thr264=
ENST00000352690.9:c.791C= MANE Select	ENSP00000342040.3:p.Thr264=
NM_001318889.1:c.791C=	NP_001305818.1:p.Thr264=
NM_001318889.2:c.791C=	NP_001305818.1:p.Thr264=
NM_005816.4:c.791C=	NP_005807.1:p.Thr264=
NM_198196.2:c.839C=	NP_937839.1:p.Thr280=
NM_198196.3:c.839C=	NP_937839.1:p.Thr280=
NR_134917.1:n.961C=
NR_134917.2:n.843C=
ENST00000283285.10:c.839C=	ENSP00000283285.5:p.Thr280=
ENST00000283285.9:c.839C=	ENSP00000283285.5:p.Thr280=
ENST00000352690.8:c.791C=	ENSP00000342040.3:p.Thr264=
ENST00000438817.6:c.791C=	ENSP00000389801.2:p.Thr264=
ENST00000494798.1:c.791C=	ENSP00000417152.1:p.Thr264=
XM_005247063.2:c.839C=	XP_005247120.1:p.Thr280=
XM_005247063.3:c.839C=	XP_005247120.1:p.Thr280=
XM_006713469.2:c.839C=	XP_006713532.1:p.Thr280=
XM_006713469.3:c.839C=	XP_006713532.1:p.Thr280=
XM_006713470.2:c.791C=	XP_006713533.1:p.Thr264=
XM_006713470.3:c.791C=	XP_006713533.1:p.Thr264=
XM_017005521.1:c.839C=	XP_016861010.1:p.Thr280=
XM_017005522.1:c.544-12758C=	XP_016861011.1:n.544-12758C=
XR_001739977.1:n.970C=
XR_241462.1:n.970C=
XR_241466.1:n.922C=
XR_924089.1:n.970C=
XR_924090.1:n.970C=