Canonical Allele Identifier: CA2279278068
Gene: TBCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82924954A= , CM000679.2:g.82924954A= GRCh38
NC_000017.10:g.80882830A= , CM000679.1:g.80882830A= GRCh37
NC_000017.9:g.78476119A= NCBI36
NG_011721.1:g.177891A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1484A=
ENST00000576677.6:n.1405A=
ENST00000681983.1:n.2412A=
ENST00000682099.1:n.1173A=
ENST00000682213.1:c.*247A= ENSP00000508166.1:n.*247A=
ENST00000682315.1:c.590A= ENSP00000507232.1:p.Gln197=
ENST00000682479.1:c.2366A= ENSP00000508214.1:p.Gln789=
ENST00000682610.1:n.1516A=
ENST00000682654.1:c.*247A= ENSP00000507412.1:n.*247A=
ENST00000682722.1:c.2225A= ENSP00000508364.1:p.Gln742=
ENST00000683041.1:c.*247A= ENSP00000506994.1:n.*247A=
ENST00000683184.1:c.*1929A= ENSP00000507757.1:n.*1929A=
ENST00000683282.1:c.2192A= ENSP00000506913.1:p.Gln731=
ENST00000683444.1:c.*1853A= ENSP00000507553.1:n.*1853A=
ENST00000683584.1:n.1099A=
ENST00000683821.1:c.590A= ENSP00000507651.1:p.Gln197=
ENST00000683839.1:n.1730A=
ENST00000684000.1:c.2360A= ENSP00000506795.1:p.Gln787=
ENST00000684188.1:c.2087A= ENSP00000507153.1:p.Gln696=
ENST00000684349.1:c.2462A= ENSP00000508067.1:p.Gln821=
ENST00000684361.1:c.2276A= ENSP00000507364.1:p.Gln759=
ENST00000684408.1:c.1919A= ENSP00000506837.1:p.Gln640=
ENST00000684429.1:c.2204A= ENSP00000507224.1:p.Gln735=
ENST00000684464.1:c.2369A= ENSP00000508333.1:p.Gln790=
ENST00000684544.1:c.2195A= ENSP00000507337.1:p.Gln732=
ENST00000684559.1:n.1031A=
ENST00000684760.1:c.2543A= ENSP00000507696.1:p.Gln848=
ENST00000684776.1:c.*759A= ENSP00000507861.1:n.*759A=
ENST00000355528.9:c.2276A= MANE Select ENSP00000347719.4:p.Gln759=
ENST00000355528.8:c.2276A= ENSP00000347719.4:p.Gln759=
ENST00000539345.6:c.2276A= ENSP00000440671.2:p.Gln759=
ENST00000571618.5:n.454A=
ENST00000571796.5:n.934A=
ENST00000574422.1:c.590A= ENSP00000458599.1:p.Gln197=
ENST00000574818.5:n.334A=
ENST00000574886.1:n.660A=
ENST00000574975.5:c.653A= ENSP00000461680.1:p.Gln218=
ENST00000576760.5:c.590A= ENSP00000460949.1:p.Gln197=
NM_005993.4:c.2276A= NP_005984.3:p.Gln759=
XM_005256396.3:c.2225A= XP_005256453.1:p.Gln742=
XM_005256399.3:c.992A= XP_005256456.1:p.Gln331=
XM_005256400.3:c.590A= XP_005256457.1:p.Gln197=
XM_005256401.3:c.590A= XP_005256458.1:p.Gln197=
XM_005256402.3:c.590A= XP_005256459.1:p.Gln197=
XM_005256403.3:c.590A= XP_005256460.1:p.Gln197=
XM_005256404.3:c.590A= XP_005256461.1:p.Gln197=
XM_006722290.2:c.2195A= XP_006722353.1:p.Gln732=
XM_006722291.2:c.980A= XP_006722354.1:p.Gln327=
XM_006722292.2:c.590A= XP_006722355.1:p.Gln197=
XM_011523589.1:c.1931A= XP_011521891.1:p.Gln644=
XM_011523590.1:c.1919A= XP_011521892.1:p.Gln640=
XM_011523591.1:c.1916A= XP_011521893.1:p.Gln639=
XM_011523592.1:c.1829A= XP_011521894.1:p.Gln610=
XM_011523593.1:c.1523A= XP_011521895.1:p.Gln508=
XM_011523594.1:c.1004A= XP_011521896.1:p.Gln335=
XM_011523595.1:c.971A= XP_011521897.1:p.Gln324=
XM_011523596.1:c.*7A= XP_011521898.1:n.*7A=
XM_011523597.1:c.737A= XP_011521899.1:p.Gln246=
XM_011523598.1:c.734A= XP_011521900.1:p.Gln245=
XM_011523599.1:c.728A= XP_011521901.1:p.Gln243=
XM_011523600.1:c.590A= XP_011521902.1:p.Gln197=
XR_430033.2:n.2384A=
XM_005256396.4:c.2225A= XP_005256453.1:p.Gln742=
XM_005256399.5:c.992A= XP_005256456.1:p.Gln331=
XM_005256404.4:c.590A= XP_005256461.1:p.Gln197=
XM_006722291.4:c.980A= XP_006722354.1:p.Gln327=
XM_006722292.3:c.590A= XP_006722355.1:p.Gln197=
XM_011523589.2:c.1931A= XP_011521891.1:p.Gln644=
XM_011523591.2:c.1916A= XP_011521893.1:p.Gln639=
XM_011523593.2:c.1523A= XP_011521895.1:p.Gln508=
XM_011523594.2:c.1004A= XP_011521896.1:p.Gln335=
XM_011523595.3:c.971A= XP_011521897.1:p.Gln324=
XM_011523597.2:c.737A= XP_011521899.1:p.Gln246=
XM_011523599.2:c.728A= XP_011521901.1:p.Gln243=
XM_011523600.3:c.590A= XP_011521902.1:p.Gln197=
XM_017024987.1:c.2087A= XP_016880476.1:p.Gln696=
XM_017024989.1:c.638A= XP_016880478.1:p.Gln213=
XM_017024990.2:c.590A= XP_016880479.1:p.Gln197=
XM_024450899.1:c.590A= XP_024306667.1:p.Gln197=
XM_024450900.1:c.590A= XP_024306668.1:p.Gln197=
XM_024450901.1:c.590A= XP_024306669.1:p.Gln197=
XM_024450902.1:c.590A= XP_024306670.1:p.Gln197=
XR_001752597.1:n.2384A=
XR_001752598.1:n.2384A=
XR_001752599.1:n.2384A=
XR_001752600.1:n.2302A=
NM_005993.5:c.2276A= MANE Select NP_005984.3:p.Gln759=