Canonical Allele Identifier: CA2279278098
Gene: TBCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82925012C= , CM000679.2:g.82925012C= GRCh38
NC_000017.10:g.80882888C= , CM000679.1:g.80882888C= GRCh37
NC_000017.9:g.78476177C= NCBI36
NG_011721.1:g.177949C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1542C=
ENST00000576677.6:n.1463C=
ENST00000681983.1:n.2470C=
ENST00000682099.1:n.1231C=
ENST00000682213.1:c.*305C= ENSP00000508166.1:n.*305C=
ENST00000682315.1:c.648C= ENSP00000507232.1:p.Ala216=
ENST00000682479.1:c.2424C= ENSP00000508214.1:p.Ala808=
ENST00000682610.1:n.1574C=
ENST00000682654.1:c.*305C= ENSP00000507412.1:n.*305C=
ENST00000682722.1:c.2283C= ENSP00000508364.1:p.Ala761=
ENST00000683041.1:c.*305C= ENSP00000506994.1:n.*305C=
ENST00000683184.1:c.*1987C= ENSP00000507757.1:n.*1987C=
ENST00000683282.1:c.2250C= ENSP00000506913.1:p.Ala750=
ENST00000683444.1:c.*1911C= ENSP00000507553.1:n.*1911C=
ENST00000683584.1:n.1157C=
ENST00000683821.1:c.648C= ENSP00000507651.1:p.Ala216=
ENST00000683839.1:n.1788C=
ENST00000684000.1:c.2418C= ENSP00000506795.1:p.Ala806=
ENST00000684188.1:c.2145C= ENSP00000507153.1:p.Ala715=
ENST00000684349.1:c.2520C= ENSP00000508067.1:p.Ala840=
ENST00000684361.1:c.2334C= ENSP00000507364.1:p.Ala778=
ENST00000684408.1:c.1977C= ENSP00000506837.1:p.Ala659=
ENST00000684429.1:c.2262C= ENSP00000507224.1:p.Ala754=
ENST00000684464.1:c.2427C= ENSP00000508333.1:p.Ala809=
ENST00000684544.1:c.2253C= ENSP00000507337.1:p.Ala751=
ENST00000684559.1:n.1089C=
ENST00000684760.1:c.2601C= ENSP00000507696.1:p.Ala867=
ENST00000684776.1:c.*817C= ENSP00000507861.1:n.*817C=
ENST00000355528.9:c.2334C= MANE Select ENSP00000347719.4:p.Ala778=
ENST00000355528.8:c.2334C= ENSP00000347719.4:p.Ala778=
ENST00000539345.6:c.2334C= ENSP00000440671.2:p.Ala778=
ENST00000571618.5:n.512C=
ENST00000571796.5:n.992C=
ENST00000574422.1:c.648C= ENSP00000458599.1:p.Ala216=
ENST00000574818.5:n.392C=
ENST00000574886.1:n.718C=
ENST00000574975.5:c.711C= ENSP00000461680.1:p.Ala237=
ENST00000576760.5:c.648C= ENSP00000460949.1:p.Ala216=
NM_005993.4:c.2334C= NP_005984.3:p.Ala778=
XM_005256396.3:c.2283C= XP_005256453.1:p.Ala761=
XM_005256399.3:c.1050C= XP_005256456.1:p.Ala350=
XM_005256400.3:c.648C= XP_005256457.1:p.Ala216=
XM_005256401.3:c.648C= XP_005256458.1:p.Ala216=
XM_005256402.3:c.648C= XP_005256459.1:p.Ala216=
XM_005256403.3:c.648C= XP_005256460.1:p.Ala216=
XM_005256404.3:c.648C= XP_005256461.1:p.Ala216=
XM_006722290.2:c.2253C= XP_006722353.1:p.Ala751=
XM_006722291.2:c.1038C= XP_006722354.1:p.Ala346=
XM_006722292.2:c.648C= XP_006722355.1:p.Ala216=
XM_011523589.1:c.1989C= XP_011521891.1:p.Ala663=
XM_011523590.1:c.1977C= XP_011521892.1:p.Ala659=
XM_011523591.1:c.1974C= XP_011521893.1:p.Ala658=
XM_011523592.1:c.1887C= XP_011521894.1:p.Ala629=
XM_011523593.1:c.1581C= XP_011521895.1:p.Ala527=
XM_011523594.1:c.1062C= XP_011521896.1:p.Ala354=
XM_011523595.1:c.1029C= XP_011521897.1:p.Ala343=
XM_011523596.1:c.*65C= XP_011521898.1:n.*65C=
XM_011523597.1:c.795C= XP_011521899.1:p.Ala265=
XM_011523598.1:c.792C= XP_011521900.1:p.Ala264=
XM_011523599.1:c.786C= XP_011521901.1:p.Ala262=
XM_011523600.1:c.648C= XP_011521902.1:p.Ala216=
XR_430033.2:n.2442C=
XM_005256396.4:c.2283C= XP_005256453.1:p.Ala761=
XM_005256399.5:c.1050C= XP_005256456.1:p.Ala350=
XM_005256404.4:c.648C= XP_005256461.1:p.Ala216=
XM_006722291.4:c.1038C= XP_006722354.1:p.Ala346=
XM_006722292.3:c.648C= XP_006722355.1:p.Ala216=
XM_011523589.2:c.1989C= XP_011521891.1:p.Ala663=
XM_011523591.2:c.1974C= XP_011521893.1:p.Ala658=
XM_011523593.2:c.1581C= XP_011521895.1:p.Ala527=
XM_011523594.2:c.1062C= XP_011521896.1:p.Ala354=
XM_011523595.3:c.1029C= XP_011521897.1:p.Ala343=
XM_011523597.2:c.795C= XP_011521899.1:p.Ala265=
XM_011523599.2:c.786C= XP_011521901.1:p.Ala262=
XM_011523600.3:c.648C= XP_011521902.1:p.Ala216=
XM_017024987.1:c.2145C= XP_016880476.1:p.Ala715=
XM_017024989.1:c.696C= XP_016880478.1:p.Ala232=
XM_017024990.2:c.648C= XP_016880479.1:p.Ala216=
XM_024450899.1:c.648C= XP_024306667.1:p.Ala216=
XM_024450900.1:c.648C= XP_024306668.1:p.Ala216=
XM_024450901.1:c.648C= XP_024306669.1:p.Ala216=
XM_024450902.1:c.648C= XP_024306670.1:p.Ala216=
XR_001752597.1:n.2442C=
XR_001752598.1:n.2442C=
XR_001752599.1:n.2442C=
XR_001752600.1:n.2360C=
NM_005993.5:c.2334C= MANE Select NP_005984.3:p.Ala778=