Canonical Allele Identifier: CA116979

Gene: CD96

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_005816.5:c.791C>T MANE Select	NP_005807.1:p.Thr264Met
ENST00000352690.9:c.791C>T MANE Select	ENSP00000342040.3:p.Thr264Met
NM_001318889.1:c.791C>T	NP_001305818.1:p.Thr264Met
NM_001318889.2:c.791C>T	NP_001305818.1:p.Thr264Met
NM_005816.4:c.791C>T	NP_005807.1:p.Thr264Met
NM_198196.2:c.839C>T	NP_937839.1:p.Thr280Met
NM_198196.3:c.839C>T	NP_937839.1:p.Thr280Met
NR_134917.1:n.961C>T
NR_134917.2:n.843C>T
ENST00000283285.10:c.839C>T	ENSP00000283285.5:p.Thr280Met
ENST00000283285.9:c.839C>T	ENSP00000283285.5:p.Thr280Met
ENST00000352690.8:c.791C>T	ENSP00000342040.3:p.Thr264Met
ENST00000438817.6:c.791C>T	ENSP00000389801.2:p.Thr264Met
ENST00000494798.1:c.791C>T	ENSP00000417152.1:p.Thr264Met
XM_005247063.2:c.839C>T	XP_005247120.1:p.Thr280Met
XM_005247063.3:c.839C>T	XP_005247120.1:p.Thr280Met
XM_006713469.2:c.839C>T	XP_006713532.1:p.Thr280Met
XM_006713469.3:c.839C>T	XP_006713532.1:p.Thr280Met
XM_006713470.2:c.791C>T	XP_006713533.1:p.Thr264Met
XM_006713470.3:c.791C>T	XP_006713533.1:p.Thr264Met
XM_017005521.1:c.839C>T	XP_016861010.1:p.Thr280Met
XM_017005522.1:c.544-12758C>T	XP_016861011.1:n.544-12758C>T
XR_001739977.1:n.970C>T
XR_241462.1:n.970C>T
XR_241466.1:n.922C>T
XR_924089.1:n.970C>T
XR_924090.1:n.970C>T