Canonical Allele Identifier: CA401633349
Gene: TBCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82924976C>G , CM000679.2:g.82924976C>G GRCh38
NC_000017.10:g.80882852C>G , CM000679.1:g.80882852C>G GRCh37
NC_000017.9:g.78476141C>G NCBI36
NG_011721.1:g.177913C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1506C>G
ENST00000576677.6:n.1427C>G
ENST00000681983.1:n.2434C>G
ENST00000682099.1:n.1195C>G
ENST00000682213.1:c.*269C>G ENSP00000508166.1:n.*269C>G
ENST00000682315.1:c.612C>G ENSP00000507232.1:p.Asn204Lys
ENST00000682479.1:c.2388C>G ENSP00000508214.1:p.Asn796Lys
ENST00000682610.1:n.1538C>G
ENST00000682654.1:c.*269C>G ENSP00000507412.1:n.*269C>G
ENST00000682722.1:c.2247C>G ENSP00000508364.1:p.Asn749Lys
ENST00000683041.1:c.*269C>G ENSP00000506994.1:n.*269C>G
ENST00000683184.1:c.*1951C>G ENSP00000507757.1:n.*1951C>G
ENST00000683282.1:c.2214C>G ENSP00000506913.1:p.Asn738Lys
ENST00000683444.1:c.*1875C>G ENSP00000507553.1:n.*1875C>G
ENST00000683584.1:n.1121C>G
ENST00000683821.1:c.612C>G ENSP00000507651.1:p.Asn204Lys
ENST00000683839.1:n.1752C>G
ENST00000684000.1:c.2382C>G ENSP00000506795.1:p.Asn794Lys
ENST00000684188.1:c.2109C>G ENSP00000507153.1:p.Asn703Lys
ENST00000684349.1:c.2484C>G ENSP00000508067.1:p.Asn828Lys
ENST00000684361.1:c.2298C>G ENSP00000507364.1:p.Asn766Lys
ENST00000684408.1:c.1941C>G ENSP00000506837.1:p.Asn647Lys
ENST00000684429.1:c.2226C>G ENSP00000507224.1:p.Asn742Lys
ENST00000684464.1:c.2391C>G ENSP00000508333.1:p.Asn797Lys
ENST00000684544.1:c.2217C>G ENSP00000507337.1:p.Asn739Lys
ENST00000684559.1:n.1053C>G
ENST00000684760.1:c.2565C>G ENSP00000507696.1:p.Asn855Lys
ENST00000684776.1:c.*781C>G ENSP00000507861.1:n.*781C>G
ENST00000355528.9:c.2298C>G MANE Select ENSP00000347719.4:p.Asn766Lys
ENST00000355528.8:c.2298C>G ENSP00000347719.4:p.Asn766Lys
ENST00000539345.6:c.2298C>G ENSP00000440671.2:p.Asn766Lys
ENST00000571618.5:n.476C>G
ENST00000571796.5:n.956C>G
ENST00000574422.1:c.612C>G ENSP00000458599.1:p.Asn204Lys
ENST00000574818.5:n.356C>G
ENST00000574886.1:n.682C>G
ENST00000574975.5:c.675C>G ENSP00000461680.1:p.Asn225Lys
ENST00000576760.5:c.612C>G ENSP00000460949.1:p.Asn204Lys
NM_005993.4:c.2298C>G NP_005984.3:p.Asn766Lys
XM_005256396.3:c.2247C>G XP_005256453.1:p.Asn749Lys
XM_005256399.3:c.1014C>G XP_005256456.1:p.Asn338Lys
XM_005256400.3:c.612C>G XP_005256457.1:p.Asn204Lys
XM_005256401.3:c.612C>G XP_005256458.1:p.Asn204Lys
XM_005256402.3:c.612C>G XP_005256459.1:p.Asn204Lys
XM_005256403.3:c.612C>G XP_005256460.1:p.Asn204Lys
XM_005256404.3:c.612C>G XP_005256461.1:p.Asn204Lys
XM_006722290.2:c.2217C>G XP_006722353.1:p.Asn739Lys
XM_006722291.2:c.1002C>G XP_006722354.1:p.Asn334Lys
XM_006722292.2:c.612C>G XP_006722355.1:p.Asn204Lys
XM_011523589.1:c.1953C>G XP_011521891.1:p.Asn651Lys
XM_011523590.1:c.1941C>G XP_011521892.1:p.Asn647Lys
XM_011523591.1:c.1938C>G XP_011521893.1:p.Asn646Lys
XM_011523592.1:c.1851C>G XP_011521894.1:p.Asn617Lys
XM_011523593.1:c.1545C>G XP_011521895.1:p.Asn515Lys
XM_011523594.1:c.1026C>G XP_011521896.1:p.Asn342Lys
XM_011523595.1:c.993C>G XP_011521897.1:p.Asn331Lys
XM_011523596.1:c.*29C>G XP_011521898.1:n.*29C>G
XM_011523597.1:c.759C>G XP_011521899.1:p.Asn253Lys
XM_011523598.1:c.756C>G XP_011521900.1:p.Asn252Lys
XM_011523599.1:c.750C>G XP_011521901.1:p.Asn250Lys
XM_011523600.1:c.612C>G XP_011521902.1:p.Asn204Lys
XR_430033.2:n.2406C>G
XM_005256396.4:c.2247C>G XP_005256453.1:p.Asn749Lys
XM_005256399.5:c.1014C>G XP_005256456.1:p.Asn338Lys
XM_005256404.4:c.612C>G XP_005256461.1:p.Asn204Lys
XM_006722291.4:c.1002C>G XP_006722354.1:p.Asn334Lys
XM_006722292.3:c.612C>G XP_006722355.1:p.Asn204Lys
XM_011523589.2:c.1953C>G XP_011521891.1:p.Asn651Lys
XM_011523591.2:c.1938C>G XP_011521893.1:p.Asn646Lys
XM_011523593.2:c.1545C>G XP_011521895.1:p.Asn515Lys
XM_011523594.2:c.1026C>G XP_011521896.1:p.Asn342Lys
XM_011523595.3:c.993C>G XP_011521897.1:p.Asn331Lys
XM_011523597.2:c.759C>G XP_011521899.1:p.Asn253Lys
XM_011523599.2:c.750C>G XP_011521901.1:p.Asn250Lys
XM_011523600.3:c.612C>G XP_011521902.1:p.Asn204Lys
XM_017024987.1:c.2109C>G XP_016880476.1:p.Asn703Lys
XM_017024989.1:c.660C>G XP_016880478.1:p.Asn220Lys
XM_017024990.2:c.612C>G XP_016880479.1:p.Asn204Lys
XM_024450899.1:c.612C>G XP_024306667.1:p.Asn204Lys
XM_024450900.1:c.612C>G XP_024306668.1:p.Asn204Lys
XM_024450901.1:c.612C>G XP_024306669.1:p.Asn204Lys
XM_024450902.1:c.612C>G XP_024306670.1:p.Asn204Lys
XR_001752597.1:n.2406C>G
XR_001752598.1:n.2406C>G
XR_001752599.1:n.2406C>G
XR_001752600.1:n.2324C>G
NM_005993.5:c.2298C>G MANE Select NP_005984.3:p.Asn766Lys