Canonical Allele Identifier: CA401633344
Gene: TBCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82924975A>G , CM000679.2:g.82924975A>G GRCh38
NC_000017.10:g.80882851A>G , CM000679.1:g.80882851A>G GRCh37
NC_000017.9:g.78476140A>G NCBI36
NG_011721.1:g.177912A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1505A>G
ENST00000576677.6:n.1426A>G
ENST00000681983.1:n.2433A>G
ENST00000682099.1:n.1194A>G
ENST00000682213.1:c.*268A>G ENSP00000508166.1:n.*268A>G
ENST00000682315.1:c.611A>G ENSP00000507232.1:p.Asn204Ser
ENST00000682479.1:c.2387A>G ENSP00000508214.1:p.Asn796Ser
ENST00000682610.1:n.1537A>G
ENST00000682654.1:c.*268A>G ENSP00000507412.1:n.*268A>G
ENST00000682722.1:c.2246A>G ENSP00000508364.1:p.Asn749Ser
ENST00000683041.1:c.*268A>G ENSP00000506994.1:n.*268A>G
ENST00000683184.1:c.*1950A>G ENSP00000507757.1:n.*1950A>G
ENST00000683282.1:c.2213A>G ENSP00000506913.1:p.Asn738Ser
ENST00000683444.1:c.*1874A>G ENSP00000507553.1:n.*1874A>G
ENST00000683584.1:n.1120A>G
ENST00000683821.1:c.611A>G ENSP00000507651.1:p.Asn204Ser
ENST00000683839.1:n.1751A>G
ENST00000684000.1:c.2381A>G ENSP00000506795.1:p.Asn794Ser
ENST00000684188.1:c.2108A>G ENSP00000507153.1:p.Asn703Ser
ENST00000684349.1:c.2483A>G ENSP00000508067.1:p.Asn828Ser
ENST00000684361.1:c.2297A>G ENSP00000507364.1:p.Asn766Ser
ENST00000684408.1:c.1940A>G ENSP00000506837.1:p.Asn647Ser
ENST00000684429.1:c.2225A>G ENSP00000507224.1:p.Asn742Ser
ENST00000684464.1:c.2390A>G ENSP00000508333.1:p.Asn797Ser
ENST00000684544.1:c.2216A>G ENSP00000507337.1:p.Asn739Ser
ENST00000684559.1:n.1052A>G
ENST00000684760.1:c.2564A>G ENSP00000507696.1:p.Asn855Ser
ENST00000684776.1:c.*780A>G ENSP00000507861.1:n.*780A>G
ENST00000355528.9:c.2297A>G MANE Select ENSP00000347719.4:p.Asn766Ser
ENST00000355528.8:c.2297A>G ENSP00000347719.4:p.Asn766Ser
ENST00000539345.6:c.2297A>G ENSP00000440671.2:p.Asn766Ser
ENST00000571618.5:n.475A>G
ENST00000571796.5:n.955A>G
ENST00000574422.1:c.611A>G ENSP00000458599.1:p.Asn204Ser
ENST00000574818.5:n.355A>G
ENST00000574886.1:n.681A>G
ENST00000574975.5:c.674A>G ENSP00000461680.1:p.Asn225Ser
ENST00000576760.5:c.611A>G ENSP00000460949.1:p.Asn204Ser
NM_005993.4:c.2297A>G NP_005984.3:p.Asn766Ser
XM_005256396.3:c.2246A>G XP_005256453.1:p.Asn749Ser
XM_005256399.3:c.1013A>G XP_005256456.1:p.Asn338Ser
XM_005256400.3:c.611A>G XP_005256457.1:p.Asn204Ser
XM_005256401.3:c.611A>G XP_005256458.1:p.Asn204Ser
XM_005256402.3:c.611A>G XP_005256459.1:p.Asn204Ser
XM_005256403.3:c.611A>G XP_005256460.1:p.Asn204Ser
XM_005256404.3:c.611A>G XP_005256461.1:p.Asn204Ser
XM_006722290.2:c.2216A>G XP_006722353.1:p.Asn739Ser
XM_006722291.2:c.1001A>G XP_006722354.1:p.Asn334Ser
XM_006722292.2:c.611A>G XP_006722355.1:p.Asn204Ser
XM_011523589.1:c.1952A>G XP_011521891.1:p.Asn651Ser
XM_011523590.1:c.1940A>G XP_011521892.1:p.Asn647Ser
XM_011523591.1:c.1937A>G XP_011521893.1:p.Asn646Ser
XM_011523592.1:c.1850A>G XP_011521894.1:p.Asn617Ser
XM_011523593.1:c.1544A>G XP_011521895.1:p.Asn515Ser
XM_011523594.1:c.1025A>G XP_011521896.1:p.Asn342Ser
XM_011523595.1:c.992A>G XP_011521897.1:p.Asn331Ser
XM_011523596.1:c.*28A>G XP_011521898.1:n.*28A>G
XM_011523597.1:c.758A>G XP_011521899.1:p.Asn253Ser
XM_011523598.1:c.755A>G XP_011521900.1:p.Asn252Ser
XM_011523599.1:c.749A>G XP_011521901.1:p.Asn250Ser
XM_011523600.1:c.611A>G XP_011521902.1:p.Asn204Ser
XR_430033.2:n.2405A>G
XM_005256396.4:c.2246A>G XP_005256453.1:p.Asn749Ser
XM_005256399.5:c.1013A>G XP_005256456.1:p.Asn338Ser
XM_005256404.4:c.611A>G XP_005256461.1:p.Asn204Ser
XM_006722291.4:c.1001A>G XP_006722354.1:p.Asn334Ser
XM_006722292.3:c.611A>G XP_006722355.1:p.Asn204Ser
XM_011523589.2:c.1952A>G XP_011521891.1:p.Asn651Ser
XM_011523591.2:c.1937A>G XP_011521893.1:p.Asn646Ser
XM_011523593.2:c.1544A>G XP_011521895.1:p.Asn515Ser
XM_011523594.2:c.1025A>G XP_011521896.1:p.Asn342Ser
XM_011523595.3:c.992A>G XP_011521897.1:p.Asn331Ser
XM_011523597.2:c.758A>G XP_011521899.1:p.Asn253Ser
XM_011523599.2:c.749A>G XP_011521901.1:p.Asn250Ser
XM_011523600.3:c.611A>G XP_011521902.1:p.Asn204Ser
XM_017024987.1:c.2108A>G XP_016880476.1:p.Asn703Ser
XM_017024989.1:c.659A>G XP_016880478.1:p.Asn220Ser
XM_017024990.2:c.611A>G XP_016880479.1:p.Asn204Ser
XM_024450899.1:c.611A>G XP_024306667.1:p.Asn204Ser
XM_024450900.1:c.611A>G XP_024306668.1:p.Asn204Ser
XM_024450901.1:c.611A>G XP_024306669.1:p.Asn204Ser
XM_024450902.1:c.611A>G XP_024306670.1:p.Asn204Ser
XR_001752597.1:n.2405A>G
XR_001752598.1:n.2405A>G
XR_001752599.1:n.2405A>G
XR_001752600.1:n.2323A>G
NM_005993.5:c.2297A>G MANE Select NP_005984.3:p.Asn766Ser