Canonical Allele Identifier: CA401633403
Gene: TBCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82924987T>A , CM000679.2:g.82924987T>A GRCh38
NC_000017.10:g.80882863T>A , CM000679.1:g.80882863T>A GRCh37
NC_000017.9:g.78476152T>A NCBI36
NG_011721.1:g.177924T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1517T>A
ENST00000576677.6:n.1438T>A
ENST00000681983.1:n.2445T>A
ENST00000682099.1:n.1206T>A
ENST00000682213.1:c.*280T>A ENSP00000508166.1:n.*280T>A
ENST00000682315.1:c.623T>A ENSP00000507232.1:p.Met208Lys
ENST00000682479.1:c.2399T>A ENSP00000508214.1:p.Met800Lys
ENST00000682610.1:n.1549T>A
ENST00000682654.1:c.*280T>A ENSP00000507412.1:n.*280T>A
ENST00000682722.1:c.2258T>A ENSP00000508364.1:p.Met753Lys
ENST00000683041.1:c.*280T>A ENSP00000506994.1:n.*280T>A
ENST00000683184.1:c.*1962T>A ENSP00000507757.1:n.*1962T>A
ENST00000683282.1:c.2225T>A ENSP00000506913.1:p.Met742Lys
ENST00000683444.1:c.*1886T>A ENSP00000507553.1:n.*1886T>A
ENST00000683584.1:n.1132T>A
ENST00000683821.1:c.623T>A ENSP00000507651.1:p.Met208Lys
ENST00000683839.1:n.1763T>A
ENST00000684000.1:c.2393T>A ENSP00000506795.1:p.Met798Lys
ENST00000684188.1:c.2120T>A ENSP00000507153.1:p.Met707Lys
ENST00000684349.1:c.2495T>A ENSP00000508067.1:p.Met832Lys
ENST00000684361.1:c.2309T>A ENSP00000507364.1:p.Met770Lys
ENST00000684408.1:c.1952T>A ENSP00000506837.1:p.Met651Lys
ENST00000684429.1:c.2237T>A ENSP00000507224.1:p.Met746Lys
ENST00000684464.1:c.2402T>A ENSP00000508333.1:p.Met801Lys
ENST00000684544.1:c.2228T>A ENSP00000507337.1:p.Met743Lys
ENST00000684559.1:n.1064T>A
ENST00000684760.1:c.2576T>A ENSP00000507696.1:p.Met859Lys
ENST00000684776.1:c.*792T>A ENSP00000507861.1:n.*792T>A
ENST00000355528.9:c.2309T>A MANE Select ENSP00000347719.4:p.Met770Lys
ENST00000355528.8:c.2309T>A ENSP00000347719.4:p.Met770Lys
ENST00000539345.6:c.2309T>A ENSP00000440671.2:p.Met770Lys
ENST00000571618.5:n.487T>A
ENST00000571796.5:n.967T>A
ENST00000574422.1:c.623T>A ENSP00000458599.1:p.Met208Lys
ENST00000574818.5:n.367T>A
ENST00000574886.1:n.693T>A
ENST00000574975.5:c.686T>A ENSP00000461680.1:p.Met229Lys
ENST00000576760.5:c.623T>A ENSP00000460949.1:p.Met208Lys
NM_005993.4:c.2309T>A NP_005984.3:p.Met770Lys
XM_005256396.3:c.2258T>A XP_005256453.1:p.Met753Lys
XM_005256399.3:c.1025T>A XP_005256456.1:p.Met342Lys
XM_005256400.3:c.623T>A XP_005256457.1:p.Met208Lys
XM_005256401.3:c.623T>A XP_005256458.1:p.Met208Lys
XM_005256402.3:c.623T>A XP_005256459.1:p.Met208Lys
XM_005256403.3:c.623T>A XP_005256460.1:p.Met208Lys
XM_005256404.3:c.623T>A XP_005256461.1:p.Met208Lys
XM_006722290.2:c.2228T>A XP_006722353.1:p.Met743Lys
XM_006722291.2:c.1013T>A XP_006722354.1:p.Met338Lys
XM_006722292.2:c.623T>A XP_006722355.1:p.Met208Lys
XM_011523589.1:c.1964T>A XP_011521891.1:p.Met655Lys
XM_011523590.1:c.1952T>A XP_011521892.1:p.Met651Lys
XM_011523591.1:c.1949T>A XP_011521893.1:p.Met650Lys
XM_011523592.1:c.1862T>A XP_011521894.1:p.Met621Lys
XM_011523593.1:c.1556T>A XP_011521895.1:p.Met519Lys
XM_011523594.1:c.1037T>A XP_011521896.1:p.Met346Lys
XM_011523595.1:c.1004T>A XP_011521897.1:p.Met335Lys
XM_011523596.1:c.*40T>A XP_011521898.1:n.*40T>A
XM_011523597.1:c.770T>A XP_011521899.1:p.Met257Lys
XM_011523598.1:c.767T>A XP_011521900.1:p.Met256Lys
XM_011523599.1:c.761T>A XP_011521901.1:p.Met254Lys
XM_011523600.1:c.623T>A XP_011521902.1:p.Met208Lys
XR_430033.2:n.2417T>A
XM_005256396.4:c.2258T>A XP_005256453.1:p.Met753Lys
XM_005256399.5:c.1025T>A XP_005256456.1:p.Met342Lys
XM_005256404.4:c.623T>A XP_005256461.1:p.Met208Lys
XM_006722291.4:c.1013T>A XP_006722354.1:p.Met338Lys
XM_006722292.3:c.623T>A XP_006722355.1:p.Met208Lys
XM_011523589.2:c.1964T>A XP_011521891.1:p.Met655Lys
XM_011523591.2:c.1949T>A XP_011521893.1:p.Met650Lys
XM_011523593.2:c.1556T>A XP_011521895.1:p.Met519Lys
XM_011523594.2:c.1037T>A XP_011521896.1:p.Met346Lys
XM_011523595.3:c.1004T>A XP_011521897.1:p.Met335Lys
XM_011523597.2:c.770T>A XP_011521899.1:p.Met257Lys
XM_011523599.2:c.761T>A XP_011521901.1:p.Met254Lys
XM_011523600.3:c.623T>A XP_011521902.1:p.Met208Lys
XM_017024987.1:c.2120T>A XP_016880476.1:p.Met707Lys
XM_017024989.1:c.671T>A XP_016880478.1:p.Met224Lys
XM_017024990.2:c.623T>A XP_016880479.1:p.Met208Lys
XM_024450899.1:c.623T>A XP_024306667.1:p.Met208Lys
XM_024450900.1:c.623T>A XP_024306668.1:p.Met208Lys
XM_024450901.1:c.623T>A XP_024306669.1:p.Met208Lys
XM_024450902.1:c.623T>A XP_024306670.1:p.Met208Lys
XR_001752597.1:n.2417T>A
XR_001752598.1:n.2417T>A
XR_001752599.1:n.2417T>A
XR_001752600.1:n.2335T>A
NM_005993.5:c.2309T>A MANE Select NP_005984.3:p.Met770Lys