Canonical Allele Identifier: CA2534421

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.111593841G>C , CM000665.2:g.111593841G>C GRCh38
NC_000003.11:g.111312688G>C , CM000665.1:g.111312688G>C GRCh37
NC_000003.10:g.112795378G>C NCBI36
NG_012156.1:g.56763G>C
NG_012156.2:g.56763G>C

Transcript Alleles

HGVS Amino-acid Change
NM_005816.5:c.808-4279G>C (CD96) MANE Select NP_005807.1:n.808-4279G>C
NM_024508.5:c.361C>G (ZBED2) MANE Select NP_078784.2:p.Arg121Gly
ENST00000317012.5:c.361C>G (ZBED2) MANE Select ENSP00000321370.4:p.Arg121Gly
ENST00000352690.9:c.808-4279G>C (CD96) MANE Select ENSP00000342040.3:n.808-4279G>C
NM_001318889.1:c.808-4279G>C (CD96) NP_001305818.1:n.808-4279G>C
NM_001318889.2:c.808-4279G>C (CD96) NP_001305818.1:n.808-4279G>C
NM_005816.4:c.808-4279G>C (CD96) NP_005807.1:n.808-4279G>C
NM_024508.4:c.361C>G (ZBED2) NP_078784.2:p.Arg121Gly
NM_198196.2:c.856-4279G>C (CD96) NP_937839.1:n.856-4279G>C
NM_198196.3:c.856-4279G>C (CD96) NP_937839.1:n.856-4279G>C
NR_134917.1:n.978-4279G>C (CD96)
NR_134917.2:n.860-4279G>C (CD96)
ENST00000283285.10:c.856-4279G>C (CD96) ENSP00000283285.5:n.856-4279G>C
ENST00000283285.9:c.856-4279G>C (CD96) ENSP00000283285.5:n.856-4279G>C
ENST00000317012.4:c.361C>G (ZBED2) ENSP00000321370.4:p.Arg121Gly
ENST00000352690.8:c.808-4279G>C (CD96) ENSP00000342040.3:n.808-4279G>C
ENST00000438817.6:c.808-4279G>C (CD96) ENSP00000389801.2:n.808-4279G>C
ENST00000494798.1:c.808-4279G>C (CD96) ENSP00000417152.1:n.808-4279G>C
XM_005247063.2:c.856-4279G>C (CD96) XP_005247120.1:n.856-4279G>C
XM_005247063.3:c.856-4279G>C (CD96) XP_005247120.1:n.856-4279G>C
XM_006713469.2:c.856-4279G>C (CD96) XP_006713532.1:n.856-4279G>C
XM_006713469.3:c.856-4279G>C (CD96) XP_006713532.1:n.856-4279G>C
XM_006713470.2:c.808-4279G>C (CD96) XP_006713533.1:n.808-4279G>C
XM_006713470.3:c.808-4279G>C (CD96) XP_006713533.1:n.808-4279G>C
XM_017005521.1:c.856-4279G>C (CD96) XP_016861010.1:n.856-4279G>C
XM_017005522.1:c.544-4279G>C (CD96) XP_016861011.1:n.544-4279G>C
XR_001739977.1:n.987-4279G>C (CD96)
XR_241462.1:n.987-4279G>C (CD96)
XR_241466.1:n.939-4279G>C (CD96)
XR_924089.1:n.987-4279G>C (CD96)
XR_924090.1:n.987-4279G>C (CD96)