Canonical Allele Identifier: CA401633251
Gene: TBCD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.82924939A>G , CM000679.2:g.82924939A>G GRCh38
NC_000017.10:g.80882815A>G , CM000679.1:g.80882815A>G GRCh37
NC_000017.9:g.78476104A>G NCBI36
NG_011721.1:g.177876A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000574886.2:n.1469A>G
ENST00000576677.6:n.1390A>G
ENST00000681983.1:n.2397A>G
ENST00000682099.1:n.1158A>G
ENST00000682213.1:c.*232A>G ENSP00000508166.1:n.*232A>G
ENST00000682315.1:c.575A>G ENSP00000507232.1:p.Glu192Gly
ENST00000682479.1:c.2351A>G ENSP00000508214.1:p.Glu784Gly
ENST00000682610.1:n.1501A>G
ENST00000682654.1:c.*232A>G ENSP00000507412.1:n.*232A>G
ENST00000682722.1:c.2210A>G ENSP00000508364.1:p.Glu737Gly
ENST00000683041.1:c.*232A>G ENSP00000506994.1:n.*232A>G
ENST00000683184.1:c.*1914A>G ENSP00000507757.1:n.*1914A>G
ENST00000683282.1:c.2177A>G ENSP00000506913.1:p.Glu726Gly
ENST00000683444.1:c.*1838A>G ENSP00000507553.1:n.*1838A>G
ENST00000683584.1:n.1084A>G
ENST00000683821.1:c.575A>G ENSP00000507651.1:p.Glu192Gly
ENST00000683839.1:n.1715A>G
ENST00000684000.1:c.2345A>G ENSP00000506795.1:p.Glu782Gly
ENST00000684188.1:c.2072A>G ENSP00000507153.1:p.Glu691Gly
ENST00000684349.1:c.2447A>G ENSP00000508067.1:p.Glu816Gly
ENST00000684361.1:c.2261A>G ENSP00000507364.1:p.Glu754Gly
ENST00000684408.1:c.1904A>G ENSP00000506837.1:p.Glu635Gly
ENST00000684429.1:c.2189A>G ENSP00000507224.1:p.Glu730Gly
ENST00000684464.1:c.2354A>G ENSP00000508333.1:p.Glu785Gly
ENST00000684544.1:c.2180A>G ENSP00000507337.1:p.Glu727Gly
ENST00000684559.1:n.1016A>G
ENST00000684760.1:c.2528A>G ENSP00000507696.1:p.Glu843Gly
ENST00000684776.1:c.*744A>G ENSP00000507861.1:n.*744A>G
ENST00000355528.9:c.2261A>G MANE Select ENSP00000347719.4:p.Glu754Gly
ENST00000355528.8:c.2261A>G ENSP00000347719.4:p.Glu754Gly
ENST00000539345.6:c.2261A>G ENSP00000440671.2:p.Glu754Gly
ENST00000571618.5:n.439A>G
ENST00000571796.5:n.919A>G
ENST00000574422.1:c.575A>G ENSP00000458599.1:p.Glu192Gly
ENST00000574818.5:n.319A>G
ENST00000574886.1:n.645A>G
ENST00000574975.5:c.638A>G ENSP00000461680.1:p.Glu213Gly
ENST00000576760.5:c.575A>G ENSP00000460949.1:p.Glu192Gly
NM_005993.4:c.2261A>G NP_005984.3:p.Glu754Gly
XM_005256396.3:c.2210A>G XP_005256453.1:p.Glu737Gly
XM_005256399.3:c.977A>G XP_005256456.1:p.Glu326Gly
XM_005256400.3:c.575A>G XP_005256457.1:p.Glu192Gly
XM_005256401.3:c.575A>G XP_005256458.1:p.Glu192Gly
XM_005256402.3:c.575A>G XP_005256459.1:p.Glu192Gly
XM_005256403.3:c.575A>G XP_005256460.1:p.Glu192Gly
XM_005256404.3:c.575A>G XP_005256461.1:p.Glu192Gly
XM_006722290.2:c.2180A>G XP_006722353.1:p.Glu727Gly
XM_006722291.2:c.965A>G XP_006722354.1:p.Glu322Gly
XM_006722292.2:c.575A>G XP_006722355.1:p.Glu192Gly
XM_011523589.1:c.1916A>G XP_011521891.1:p.Glu639Gly
XM_011523590.1:c.1904A>G XP_011521892.1:p.Glu635Gly
XM_011523591.1:c.1901A>G XP_011521893.1:p.Glu634Gly
XM_011523592.1:c.1814A>G XP_011521894.1:p.Glu605Gly
XM_011523593.1:c.1508A>G XP_011521895.1:p.Glu503Gly
XM_011523594.1:c.989A>G XP_011521896.1:p.Glu330Gly
XM_011523595.1:c.956A>G XP_011521897.1:p.Glu319Gly
XM_011523596.1:c.2179A>G XP_011521898.1:p.Arg727Gly
XM_011523597.1:c.722A>G XP_011521899.1:p.Glu241Gly
XM_011523598.1:c.719A>G XP_011521900.1:p.Glu240Gly
XM_011523599.1:c.713A>G XP_011521901.1:p.Glu238Gly
XM_011523600.1:c.575A>G XP_011521902.1:p.Glu192Gly
XR_430033.2:n.2369A>G
XM_005256396.4:c.2210A>G XP_005256453.1:p.Glu737Gly
XM_005256399.5:c.977A>G XP_005256456.1:p.Glu326Gly
XM_005256404.4:c.575A>G XP_005256461.1:p.Glu192Gly
XM_006722291.4:c.965A>G XP_006722354.1:p.Glu322Gly
XM_006722292.3:c.575A>G XP_006722355.1:p.Glu192Gly
XM_011523589.2:c.1916A>G XP_011521891.1:p.Glu639Gly
XM_011523591.2:c.1901A>G XP_011521893.1:p.Glu634Gly
XM_011523593.2:c.1508A>G XP_011521895.1:p.Glu503Gly
XM_011523594.2:c.989A>G XP_011521896.1:p.Glu330Gly
XM_011523595.3:c.956A>G XP_011521897.1:p.Glu319Gly
XM_011523597.2:c.722A>G XP_011521899.1:p.Glu241Gly
XM_011523599.2:c.713A>G XP_011521901.1:p.Glu238Gly
XM_011523600.3:c.575A>G XP_011521902.1:p.Glu192Gly
XM_017024987.1:c.2072A>G XP_016880476.1:p.Glu691Gly
XM_017024989.1:c.623A>G XP_016880478.1:p.Glu208Gly
XM_017024990.2:c.575A>G XP_016880479.1:p.Glu192Gly
XM_024450899.1:c.575A>G XP_024306667.1:p.Glu192Gly
XM_024450900.1:c.575A>G XP_024306668.1:p.Glu192Gly
XM_024450901.1:c.575A>G XP_024306669.1:p.Glu192Gly
XM_024450902.1:c.575A>G XP_024306670.1:p.Glu192Gly
XR_001752597.1:n.2369A>G
XR_001752598.1:n.2369A>G
XR_001752599.1:n.2369A>G
XR_001752600.1:n.2287A>G
NM_005993.5:c.2261A>G MANE Select NP_005984.3:p.Glu754Gly