Canonical Allele Identifier: CA2279278093
Gene: TBCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82924996G= , CM000679.2:g.82924996G= GRCh38
NC_000017.10:g.80882872G= , CM000679.1:g.80882872G= GRCh37
NC_000017.9:g.78476161G= NCBI36
NG_011721.1:g.177933G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1526G=
ENST00000576677.6:n.1447G=
ENST00000681983.1:n.2454G=
ENST00000682099.1:n.1215G=
ENST00000682213.1:c.*289G= ENSP00000508166.1:n.*289G=
ENST00000682315.1:c.632G= ENSP00000507232.1:p.Cys211=
ENST00000682479.1:c.2408G= ENSP00000508214.1:p.Cys803=
ENST00000682610.1:n.1558G=
ENST00000682654.1:c.*289G= ENSP00000507412.1:n.*289G=
ENST00000682722.1:c.2267G= ENSP00000508364.1:p.Cys756=
ENST00000683041.1:c.*289G= ENSP00000506994.1:n.*289G=
ENST00000683184.1:c.*1971G= ENSP00000507757.1:n.*1971G=
ENST00000683282.1:c.2234G= ENSP00000506913.1:p.Cys745=
ENST00000683444.1:c.*1895G= ENSP00000507553.1:n.*1895G=
ENST00000683584.1:n.1141G=
ENST00000683821.1:c.632G= ENSP00000507651.1:p.Cys211=
ENST00000683839.1:n.1772G=
ENST00000684000.1:c.2402G= ENSP00000506795.1:p.Cys801=
ENST00000684188.1:c.2129G= ENSP00000507153.1:p.Cys710=
ENST00000684349.1:c.2504G= ENSP00000508067.1:p.Cys835=
ENST00000684361.1:c.2318G= ENSP00000507364.1:p.Cys773=
ENST00000684408.1:c.1961G= ENSP00000506837.1:p.Cys654=
ENST00000684429.1:c.2246G= ENSP00000507224.1:p.Cys749=
ENST00000684464.1:c.2411G= ENSP00000508333.1:p.Cys804=
ENST00000684544.1:c.2237G= ENSP00000507337.1:p.Cys746=
ENST00000684559.1:n.1073G=
ENST00000684760.1:c.2585G= ENSP00000507696.1:p.Cys862=
ENST00000684776.1:c.*801G= ENSP00000507861.1:n.*801G=
ENST00000355528.9:c.2318G= MANE Select ENSP00000347719.4:p.Cys773=
ENST00000355528.8:c.2318G= ENSP00000347719.4:p.Cys773=
ENST00000539345.6:c.2318G= ENSP00000440671.2:p.Cys773=
ENST00000571618.5:n.496G=
ENST00000571796.5:n.976G=
ENST00000574422.1:c.632G= ENSP00000458599.1:p.Cys211=
ENST00000574818.5:n.376G=
ENST00000574886.1:n.702G=
ENST00000574975.5:c.695G= ENSP00000461680.1:p.Cys232=
ENST00000576760.5:c.632G= ENSP00000460949.1:p.Cys211=
NM_005993.4:c.2318G= NP_005984.3:p.Cys773=
XM_005256396.3:c.2267G= XP_005256453.1:p.Cys756=
XM_005256399.3:c.1034G= XP_005256456.1:p.Cys345=
XM_005256400.3:c.632G= XP_005256457.1:p.Cys211=
XM_005256401.3:c.632G= XP_005256458.1:p.Cys211=
XM_005256402.3:c.632G= XP_005256459.1:p.Cys211=
XM_005256403.3:c.632G= XP_005256460.1:p.Cys211=
XM_005256404.3:c.632G= XP_005256461.1:p.Cys211=
XM_006722290.2:c.2237G= XP_006722353.1:p.Cys746=
XM_006722291.2:c.1022G= XP_006722354.1:p.Cys341=
XM_006722292.2:c.632G= XP_006722355.1:p.Cys211=
XM_011523589.1:c.1973G= XP_011521891.1:p.Cys658=
XM_011523590.1:c.1961G= XP_011521892.1:p.Cys654=
XM_011523591.1:c.1958G= XP_011521893.1:p.Cys653=
XM_011523592.1:c.1871G= XP_011521894.1:p.Cys624=
XM_011523593.1:c.1565G= XP_011521895.1:p.Cys522=
XM_011523594.1:c.1046G= XP_011521896.1:p.Cys349=
XM_011523595.1:c.1013G= XP_011521897.1:p.Cys338=
XM_011523596.1:c.*49G= XP_011521898.1:n.*49G=
XM_011523597.1:c.779G= XP_011521899.1:p.Cys260=
XM_011523598.1:c.776G= XP_011521900.1:p.Cys259=
XM_011523599.1:c.770G= XP_011521901.1:p.Cys257=
XM_011523600.1:c.632G= XP_011521902.1:p.Cys211=
XR_430033.2:n.2426G=
XM_005256396.4:c.2267G= XP_005256453.1:p.Cys756=
XM_005256399.5:c.1034G= XP_005256456.1:p.Cys345=
XM_005256404.4:c.632G= XP_005256461.1:p.Cys211=
XM_006722291.4:c.1022G= XP_006722354.1:p.Cys341=
XM_006722292.3:c.632G= XP_006722355.1:p.Cys211=
XM_011523589.2:c.1973G= XP_011521891.1:p.Cys658=
XM_011523591.2:c.1958G= XP_011521893.1:p.Cys653=
XM_011523593.2:c.1565G= XP_011521895.1:p.Cys522=
XM_011523594.2:c.1046G= XP_011521896.1:p.Cys349=
XM_011523595.3:c.1013G= XP_011521897.1:p.Cys338=
XM_011523597.2:c.779G= XP_011521899.1:p.Cys260=
XM_011523599.2:c.770G= XP_011521901.1:p.Cys257=
XM_011523600.3:c.632G= XP_011521902.1:p.Cys211=
XM_017024987.1:c.2129G= XP_016880476.1:p.Cys710=
XM_017024989.1:c.680G= XP_016880478.1:p.Cys227=
XM_017024990.2:c.632G= XP_016880479.1:p.Cys211=
XM_024450899.1:c.632G= XP_024306667.1:p.Cys211=
XM_024450900.1:c.632G= XP_024306668.1:p.Cys211=
XM_024450901.1:c.632G= XP_024306669.1:p.Cys211=
XM_024450902.1:c.632G= XP_024306670.1:p.Cys211=
XR_001752597.1:n.2426G=
XR_001752598.1:n.2426G=
XR_001752599.1:n.2426G=
XR_001752600.1:n.2344G=
NM_005993.5:c.2318G= MANE Select NP_005984.3:p.Cys773=