Canonical Allele Identifier: CA401633601

Gene: TBCD

Linked Data

• MyVariant Identifiers: chr17:g.80882909C>A (hg19) ; chr17:g.82925033C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82925033C>A , CM000679.2:g.82925033C>A	GRCh38
NC_000017.10:g.80882909C>A , CM000679.1:g.80882909C>A	GRCh37
NC_000017.9:g.78476198C>A	NCBI36
NG_011721.1:g.177970C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1563C>A
ENST00000576677.6:n.1484C>A
ENST00000681983.1:n.2491C>A
ENST00000682099.1:n.1252C>A
ENST00000682213.1:c.*326C>A	ENSP00000508166.1:n.*326C>A
ENST00000682315.1:c.669C>A	ENSP00000507232.1:p.Phe223Leu
ENST00000682479.1:c.2445C>A	ENSP00000508214.1:p.Phe815Leu
ENST00000682610.1:n.1595C>A
ENST00000682654.1:c.*326C>A	ENSP00000507412.1:n.*326C>A
ENST00000682722.1:c.2304C>A	ENSP00000508364.1:p.Phe768Leu
ENST00000683041.1:c.*326C>A	ENSP00000506994.1:n.*326C>A
ENST00000683184.1:c.*2008C>A	ENSP00000507757.1:n.*2008C>A
ENST00000683282.1:c.2271C>A	ENSP00000506913.1:p.Phe757Leu
ENST00000683444.1:c.*1932C>A	ENSP00000507553.1:n.*1932C>A
ENST00000683584.1:n.1178C>A
ENST00000683821.1:c.669C>A	ENSP00000507651.1:p.Phe223Leu
ENST00000683839.1:n.1809C>A
ENST00000684000.1:c.2439C>A	ENSP00000506795.1:p.Phe813Leu
ENST00000684188.1:c.2166C>A	ENSP00000507153.1:p.Phe722Leu
ENST00000684349.1:c.2541C>A	ENSP00000508067.1:p.Phe847Leu
ENST00000684361.1:c.2355C>A	ENSP00000507364.1:p.Phe785Leu
ENST00000684408.1:c.1998C>A	ENSP00000506837.1:p.Phe666Leu
ENST00000684429.1:c.2283C>A	ENSP00000507224.1:p.Phe761Leu
ENST00000684464.1:c.2448C>A	ENSP00000508333.1:p.Phe816Leu
ENST00000684544.1:c.2274C>A	ENSP00000507337.1:p.Phe758Leu
ENST00000684559.1:n.1110C>A
ENST00000684760.1:c.2622C>A	ENSP00000507696.1:p.Phe874Leu
ENST00000684776.1:c.*838C>A	ENSP00000507861.1:n.*838C>A
ENST00000355528.9:c.2355C>A MANE Select	ENSP00000347719.4:p.Phe785Leu
ENST00000355528.8:c.2355C>A	ENSP00000347719.4:p.Phe785Leu
ENST00000539345.6:c.2355C>A	ENSP00000440671.2:p.Phe785Leu
ENST00000571618.5:n.533C>A
ENST00000571796.5:n.1013C>A
ENST00000574422.1:c.669C>A	ENSP00000458599.1:p.Phe223Leu
ENST00000574818.5:n.413C>A
ENST00000574886.1:n.739C>A
ENST00000574975.5:c.732C>A	ENSP00000461680.1:p.Phe244Leu
ENST00000576760.5:c.669C>A	ENSP00000460949.1:p.Phe223Leu
NM_005993.4:c.2355C>A	NP_005984.3:p.Phe785Leu
XM_005256396.3:c.2304C>A	XP_005256453.1:p.Phe768Leu
XM_005256399.3:c.1071C>A	XP_005256456.1:p.Phe357Leu
XM_005256400.3:c.669C>A	XP_005256457.1:p.Phe223Leu
XM_005256401.3:c.669C>A	XP_005256458.1:p.Phe223Leu
XM_005256402.3:c.669C>A	XP_005256459.1:p.Phe223Leu
XM_005256403.3:c.669C>A	XP_005256460.1:p.Phe223Leu
XM_005256404.3:c.669C>A	XP_005256461.1:p.Phe223Leu
XM_006722290.2:c.2274C>A	XP_006722353.1:p.Phe758Leu
XM_006722291.2:c.1059C>A	XP_006722354.1:p.Phe353Leu
XM_006722292.2:c.669C>A	XP_006722355.1:p.Phe223Leu
XM_011523589.1:c.2010C>A	XP_011521891.1:p.Phe670Leu
XM_011523590.1:c.1998C>A	XP_011521892.1:p.Phe666Leu
XM_011523591.1:c.1995C>A	XP_011521893.1:p.Phe665Leu
XM_011523592.1:c.1908C>A	XP_011521894.1:p.Phe636Leu
XM_011523593.1:c.1602C>A	XP_011521895.1:p.Phe534Leu
XM_011523594.1:c.1083C>A	XP_011521896.1:p.Phe361Leu
XM_011523595.1:c.1050C>A	XP_011521897.1:p.Phe350Leu
XM_011523597.1:c.816C>A	XP_011521899.1:p.Phe272Leu
XM_011523598.1:c.813C>A	XP_011521900.1:p.Phe271Leu
XM_011523599.1:c.807C>A	XP_011521901.1:p.Phe269Leu
XM_011523600.1:c.669C>A	XP_011521902.1:p.Phe223Leu
XR_430033.2:n.2463C>A
XM_005256396.4:c.2304C>A	XP_005256453.1:p.Phe768Leu
XM_005256399.5:c.1071C>A	XP_005256456.1:p.Phe357Leu
XM_005256404.4:c.669C>A	XP_005256461.1:p.Phe223Leu
XM_006722291.4:c.1059C>A	XP_006722354.1:p.Phe353Leu
XM_006722292.3:c.669C>A	XP_006722355.1:p.Phe223Leu
XM_011523589.2:c.2010C>A	XP_011521891.1:p.Phe670Leu
XM_011523591.2:c.1995C>A	XP_011521893.1:p.Phe665Leu
XM_011523593.2:c.1602C>A	XP_011521895.1:p.Phe534Leu
XM_011523594.2:c.1083C>A	XP_011521896.1:p.Phe361Leu
XM_011523595.3:c.1050C>A	XP_011521897.1:p.Phe350Leu
XM_011523597.2:c.816C>A	XP_011521899.1:p.Phe272Leu
XM_011523599.2:c.807C>A	XP_011521901.1:p.Phe269Leu
XM_011523600.3:c.669C>A	XP_011521902.1:p.Phe223Leu
XM_017024987.1:c.2166C>A	XP_016880476.1:p.Phe722Leu
XM_017024989.1:c.717C>A	XP_016880478.1:p.Phe239Leu
XM_017024990.2:c.669C>A	XP_016880479.1:p.Phe223Leu
XM_024450899.1:c.669C>A	XP_024306667.1:p.Phe223Leu
XM_024450900.1:c.669C>A	XP_024306668.1:p.Phe223Leu
XM_024450901.1:c.669C>A	XP_024306669.1:p.Phe223Leu
XM_024450902.1:c.669C>A	XP_024306670.1:p.Phe223Leu
XR_001752597.1:n.2463C>A
XR_001752598.1:n.2463C>A
XR_001752599.1:n.2463C>A
XR_001752600.1:n.2381C>A
NM_005993.5:c.2355C>A MANE Select	NP_005984.3:p.Phe785Leu