Canonical Allele Identifier: CA2279278072
Gene: TBCD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82924963C= , CM000679.2:g.82924963C= GRCh38
NC_000017.10:g.80882839C= , CM000679.1:g.80882839C= GRCh37
NC_000017.9:g.78476128C= NCBI36
NG_011721.1:g.177900C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1493C=
ENST00000576677.6:n.1414C=
ENST00000681983.1:n.2421C=
ENST00000682099.1:n.1182C=
ENST00000682213.1:c.*256C= ENSP00000508166.1:n.*256C=
ENST00000682315.1:c.599C= ENSP00000507232.1:p.Ala200=
ENST00000682479.1:c.2375C= ENSP00000508214.1:p.Ala792=
ENST00000682610.1:n.1525C=
ENST00000682654.1:c.*256C= ENSP00000507412.1:n.*256C=
ENST00000682722.1:c.2234C= ENSP00000508364.1:p.Ala745=
ENST00000683041.1:c.*256C= ENSP00000506994.1:n.*256C=
ENST00000683184.1:c.*1938C= ENSP00000507757.1:n.*1938C=
ENST00000683282.1:c.2201C= ENSP00000506913.1:p.Ala734=
ENST00000683444.1:c.*1862C= ENSP00000507553.1:n.*1862C=
ENST00000683584.1:n.1108C=
ENST00000683821.1:c.599C= ENSP00000507651.1:p.Ala200=
ENST00000683839.1:n.1739C=
ENST00000684000.1:c.2369C= ENSP00000506795.1:p.Ala790=
ENST00000684188.1:c.2096C= ENSP00000507153.1:p.Ala699=
ENST00000684349.1:c.2471C= ENSP00000508067.1:p.Ala824=
ENST00000684361.1:c.2285C= ENSP00000507364.1:p.Ala762=
ENST00000684408.1:c.1928C= ENSP00000506837.1:p.Ala643=
ENST00000684429.1:c.2213C= ENSP00000507224.1:p.Ala738=
ENST00000684464.1:c.2378C= ENSP00000508333.1:p.Ala793=
ENST00000684544.1:c.2204C= ENSP00000507337.1:p.Ala735=
ENST00000684559.1:n.1040C=
ENST00000684760.1:c.2552C= ENSP00000507696.1:p.Ala851=
ENST00000684776.1:c.*768C= ENSP00000507861.1:n.*768C=
ENST00000355528.9:c.2285C= MANE Select ENSP00000347719.4:p.Ala762=
ENST00000355528.8:c.2285C= ENSP00000347719.4:p.Ala762=
ENST00000539345.6:c.2285C= ENSP00000440671.2:p.Ala762=
ENST00000571618.5:n.463C=
ENST00000571796.5:n.943C=
ENST00000574422.1:c.599C= ENSP00000458599.1:p.Ala200=
ENST00000574818.5:n.343C=
ENST00000574886.1:n.669C=
ENST00000574975.5:c.662C= ENSP00000461680.1:p.Ala221=
ENST00000576760.5:c.599C= ENSP00000460949.1:p.Ala200=
NM_005993.4:c.2285C= NP_005984.3:p.Ala762=
XM_005256396.3:c.2234C= XP_005256453.1:p.Ala745=
XM_005256399.3:c.1001C= XP_005256456.1:p.Ala334=
XM_005256400.3:c.599C= XP_005256457.1:p.Ala200=
XM_005256401.3:c.599C= XP_005256458.1:p.Ala200=
XM_005256402.3:c.599C= XP_005256459.1:p.Ala200=
XM_005256403.3:c.599C= XP_005256460.1:p.Ala200=
XM_005256404.3:c.599C= XP_005256461.1:p.Ala200=
XM_006722290.2:c.2204C= XP_006722353.1:p.Ala735=
XM_006722291.2:c.989C= XP_006722354.1:p.Ala330=
XM_006722292.2:c.599C= XP_006722355.1:p.Ala200=
XM_011523589.1:c.1940C= XP_011521891.1:p.Ala647=
XM_011523590.1:c.1928C= XP_011521892.1:p.Ala643=
XM_011523591.1:c.1925C= XP_011521893.1:p.Ala642=
XM_011523592.1:c.1838C= XP_011521894.1:p.Ala613=
XM_011523593.1:c.1532C= XP_011521895.1:p.Ala511=
XM_011523594.1:c.1013C= XP_011521896.1:p.Ala338=
XM_011523595.1:c.980C= XP_011521897.1:p.Ala327=
XM_011523596.1:c.*16C= XP_011521898.1:n.*16C=
XM_011523597.1:c.746C= XP_011521899.1:p.Ala249=
XM_011523598.1:c.743C= XP_011521900.1:p.Ala248=
XM_011523599.1:c.737C= XP_011521901.1:p.Ala246=
XM_011523600.1:c.599C= XP_011521902.1:p.Ala200=
XR_430033.2:n.2393C=
XM_005256396.4:c.2234C= XP_005256453.1:p.Ala745=
XM_005256399.5:c.1001C= XP_005256456.1:p.Ala334=
XM_005256404.4:c.599C= XP_005256461.1:p.Ala200=
XM_006722291.4:c.989C= XP_006722354.1:p.Ala330=
XM_006722292.3:c.599C= XP_006722355.1:p.Ala200=
XM_011523589.2:c.1940C= XP_011521891.1:p.Ala647=
XM_011523591.2:c.1925C= XP_011521893.1:p.Ala642=
XM_011523593.2:c.1532C= XP_011521895.1:p.Ala511=
XM_011523594.2:c.1013C= XP_011521896.1:p.Ala338=
XM_011523595.3:c.980C= XP_011521897.1:p.Ala327=
XM_011523597.2:c.746C= XP_011521899.1:p.Ala249=
XM_011523599.2:c.737C= XP_011521901.1:p.Ala246=
XM_011523600.3:c.599C= XP_011521902.1:p.Ala200=
XM_017024987.1:c.2096C= XP_016880476.1:p.Ala699=
XM_017024989.1:c.647C= XP_016880478.1:p.Ala216=
XM_017024990.2:c.599C= XP_016880479.1:p.Ala200=
XM_024450899.1:c.599C= XP_024306667.1:p.Ala200=
XM_024450900.1:c.599C= XP_024306668.1:p.Ala200=
XM_024450901.1:c.599C= XP_024306669.1:p.Ala200=
XM_024450902.1:c.599C= XP_024306670.1:p.Ala200=
XR_001752597.1:n.2393C=
XR_001752598.1:n.2393C=
XR_001752599.1:n.2393C=
XR_001752600.1:n.2311C=
NM_005993.5:c.2285C= MANE Select NP_005984.3:p.Ala762=