Canonical Allele Identifier: CA401633624

Gene: TBCD

Linked Data

• MyVariant Identifiers: chr17:g.80882914T>G (hg19) ; chr17:g.82925038T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82925038T>G , CM000679.2:g.82925038T>G	GRCh38
NC_000017.10:g.80882914T>G , CM000679.1:g.80882914T>G	GRCh37
NC_000017.9:g.78476203T>G	NCBI36
NG_011721.1:g.177975T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1568T>G
ENST00000576677.6:n.1489T>G
ENST00000681983.1:n.2496T>G
ENST00000682099.1:n.1257T>G
ENST00000682213.1:c.*331T>G	ENSP00000508166.1:n.*331T>G
ENST00000682315.1:c.674T>G	ENSP00000507232.1:p.Leu225Arg
ENST00000682479.1:c.2450T>G	ENSP00000508214.1:p.Leu817Arg
ENST00000682610.1:n.1600T>G
ENST00000682654.1:c.*331T>G	ENSP00000507412.1:n.*331T>G
ENST00000682722.1:c.2309T>G	ENSP00000508364.1:p.Leu770Arg
ENST00000683041.1:c.*331T>G	ENSP00000506994.1:n.*331T>G
ENST00000683184.1:c.*2013T>G	ENSP00000507757.1:n.*2013T>G
ENST00000683282.1:c.2276T>G	ENSP00000506913.1:p.Leu759Arg
ENST00000683444.1:c.*1937T>G	ENSP00000507553.1:n.*1937T>G
ENST00000683584.1:n.1183T>G
ENST00000683821.1:c.674T>G	ENSP00000507651.1:p.Leu225Arg
ENST00000683839.1:n.1814T>G
ENST00000684000.1:c.2444T>G	ENSP00000506795.1:p.Leu815Arg
ENST00000684188.1:c.2171T>G	ENSP00000507153.1:p.Leu724Arg
ENST00000684349.1:c.2546T>G	ENSP00000508067.1:p.Leu849Arg
ENST00000684361.1:c.2360T>G	ENSP00000507364.1:p.Leu787Arg
ENST00000684408.1:c.2003T>G	ENSP00000506837.1:p.Leu668Arg
ENST00000684429.1:c.2288T>G	ENSP00000507224.1:p.Leu763Arg
ENST00000684464.1:c.2453T>G	ENSP00000508333.1:p.Leu818Arg
ENST00000684544.1:c.2279T>G	ENSP00000507337.1:p.Leu760Arg
ENST00000684559.1:n.1115T>G
ENST00000684760.1:c.2627T>G	ENSP00000507696.1:p.Leu876Arg
ENST00000684776.1:c.*843T>G	ENSP00000507861.1:n.*843T>G
ENST00000355528.9:c.2360T>G MANE Select	ENSP00000347719.4:p.Leu787Arg
ENST00000355528.8:c.2360T>G	ENSP00000347719.4:p.Leu787Arg
ENST00000539345.6:c.2360T>G	ENSP00000440671.2:p.Leu787Arg
ENST00000571618.5:n.538T>G
ENST00000571796.5:n.1018T>G
ENST00000574422.1:c.674T>G	ENSP00000458599.1:p.Leu225Arg
ENST00000574818.5:n.418T>G
ENST00000574886.1:n.744T>G
ENST00000574975.5:c.737T>G	ENSP00000461680.1:p.Leu246Arg
ENST00000576760.5:c.674T>G	ENSP00000460949.1:p.Leu225Arg
NM_005993.4:c.2360T>G	NP_005984.3:p.Leu787Arg
XM_005256396.3:c.2309T>G	XP_005256453.1:p.Leu770Arg
XM_005256399.3:c.1076T>G	XP_005256456.1:p.Leu359Arg
XM_005256400.3:c.674T>G	XP_005256457.1:p.Leu225Arg
XM_005256401.3:c.674T>G	XP_005256458.1:p.Leu225Arg
XM_005256402.3:c.674T>G	XP_005256459.1:p.Leu225Arg
XM_005256403.3:c.674T>G	XP_005256460.1:p.Leu225Arg
XM_005256404.3:c.674T>G	XP_005256461.1:p.Leu225Arg
XM_006722290.2:c.2279T>G	XP_006722353.1:p.Leu760Arg
XM_006722291.2:c.1064T>G	XP_006722354.1:p.Leu355Arg
XM_006722292.2:c.674T>G	XP_006722355.1:p.Leu225Arg
XM_011523589.1:c.2015T>G	XP_011521891.1:p.Leu672Arg
XM_011523590.1:c.2003T>G	XP_011521892.1:p.Leu668Arg
XM_011523591.1:c.2000T>G	XP_011521893.1:p.Leu667Arg
XM_011523592.1:c.1913T>G	XP_011521894.1:p.Leu638Arg
XM_011523593.1:c.1607T>G	XP_011521895.1:p.Leu536Arg
XM_011523594.1:c.1088T>G	XP_011521896.1:p.Leu363Arg
XM_011523595.1:c.1055T>G	XP_011521897.1:p.Leu352Arg
XM_011523597.1:c.821T>G	XP_011521899.1:p.Leu274Arg
XM_011523598.1:c.818T>G	XP_011521900.1:p.Leu273Arg
XM_011523599.1:c.812T>G	XP_011521901.1:p.Leu271Arg
XM_011523600.1:c.674T>G	XP_011521902.1:p.Leu225Arg
XR_430033.2:n.2468T>G
XM_005256396.4:c.2309T>G	XP_005256453.1:p.Leu770Arg
XM_005256399.5:c.1076T>G	XP_005256456.1:p.Leu359Arg
XM_005256404.4:c.674T>G	XP_005256461.1:p.Leu225Arg
XM_006722291.4:c.1064T>G	XP_006722354.1:p.Leu355Arg
XM_006722292.3:c.674T>G	XP_006722355.1:p.Leu225Arg
XM_011523589.2:c.2015T>G	XP_011521891.1:p.Leu672Arg
XM_011523591.2:c.2000T>G	XP_011521893.1:p.Leu667Arg
XM_011523593.2:c.1607T>G	XP_011521895.1:p.Leu536Arg
XM_011523594.2:c.1088T>G	XP_011521896.1:p.Leu363Arg
XM_011523595.3:c.1055T>G	XP_011521897.1:p.Leu352Arg
XM_011523597.2:c.821T>G	XP_011521899.1:p.Leu274Arg
XM_011523599.2:c.812T>G	XP_011521901.1:p.Leu271Arg
XM_011523600.3:c.674T>G	XP_011521902.1:p.Leu225Arg
XM_017024987.1:c.2171T>G	XP_016880476.1:p.Leu724Arg
XM_017024989.1:c.722T>G	XP_016880478.1:p.Leu241Arg
XM_017024990.2:c.674T>G	XP_016880479.1:p.Leu225Arg
XM_024450899.1:c.674T>G	XP_024306667.1:p.Leu225Arg
XM_024450900.1:c.674T>G	XP_024306668.1:p.Leu225Arg
XM_024450901.1:c.674T>G	XP_024306669.1:p.Leu225Arg
XM_024450902.1:c.674T>G	XP_024306670.1:p.Leu225Arg
XR_001752597.1:n.2468T>G
XR_001752598.1:n.2468T>G
XR_001752599.1:n.2468T>G
XR_001752600.1:n.2386T>G
NM_005993.5:c.2360T>G MANE Select	NP_005984.3:p.Leu787Arg