Canonical Allele Identifier: CA401633533

Gene: TBCD

Linked Data

• MyVariant Identifiers: chr17:g.80882892G>C (hg19) ; chr17:g.82925016G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82925016G>C , CM000679.2:g.82925016G>C	GRCh38
NC_000017.10:g.80882892G>C , CM000679.1:g.80882892G>C	GRCh37
NC_000017.9:g.78476181G>C	NCBI36
NG_011721.1:g.177953G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1546G>C
ENST00000576677.6:n.1467G>C
ENST00000681983.1:n.2474G>C
ENST00000682099.1:n.1235G>C
ENST00000682213.1:c.*309G>C	ENSP00000508166.1:n.*309G>C
ENST00000682315.1:c.652G>C	ENSP00000507232.1:p.Gly218Arg
ENST00000682479.1:c.2428G>C	ENSP00000508214.1:p.Gly810Arg
ENST00000682610.1:n.1578G>C
ENST00000682654.1:c.*309G>C	ENSP00000507412.1:n.*309G>C
ENST00000682722.1:c.2287G>C	ENSP00000508364.1:p.Gly763Arg
ENST00000683041.1:c.*309G>C	ENSP00000506994.1:n.*309G>C
ENST00000683184.1:c.*1991G>C	ENSP00000507757.1:n.*1991G>C
ENST00000683282.1:c.2254G>C	ENSP00000506913.1:p.Gly752Arg
ENST00000683444.1:c.*1915G>C	ENSP00000507553.1:n.*1915G>C
ENST00000683584.1:n.1161G>C
ENST00000683821.1:c.652G>C	ENSP00000507651.1:p.Gly218Arg
ENST00000683839.1:n.1792G>C
ENST00000684000.1:c.2422G>C	ENSP00000506795.1:p.Gly808Arg
ENST00000684188.1:c.2149G>C	ENSP00000507153.1:p.Gly717Arg
ENST00000684349.1:c.2524G>C	ENSP00000508067.1:p.Gly842Arg
ENST00000684361.1:c.2338G>C	ENSP00000507364.1:p.Gly780Arg
ENST00000684408.1:c.1981G>C	ENSP00000506837.1:p.Gly661Arg
ENST00000684429.1:c.2266G>C	ENSP00000507224.1:p.Gly756Arg
ENST00000684464.1:c.2431G>C	ENSP00000508333.1:p.Gly811Arg
ENST00000684544.1:c.2257G>C	ENSP00000507337.1:p.Gly753Arg
ENST00000684559.1:n.1093G>C
ENST00000684760.1:c.2605G>C	ENSP00000507696.1:p.Gly869Arg
ENST00000684776.1:c.*821G>C	ENSP00000507861.1:n.*821G>C
ENST00000355528.9:c.2338G>C MANE Select	ENSP00000347719.4:p.Gly780Arg
ENST00000355528.8:c.2338G>C	ENSP00000347719.4:p.Gly780Arg
ENST00000539345.6:c.2338G>C	ENSP00000440671.2:p.Gly780Arg
ENST00000571618.5:n.516G>C
ENST00000571796.5:n.996G>C
ENST00000574422.1:c.652G>C	ENSP00000458599.1:p.Gly218Arg
ENST00000574818.5:n.396G>C
ENST00000574886.1:n.722G>C
ENST00000574975.5:c.715G>C	ENSP00000461680.1:p.Gly239Arg
ENST00000576760.5:c.652G>C	ENSP00000460949.1:p.Gly218Arg
NM_005993.4:c.2338G>C	NP_005984.3:p.Gly780Arg
XM_005256396.3:c.2287G>C	XP_005256453.1:p.Gly763Arg
XM_005256399.3:c.1054G>C	XP_005256456.1:p.Gly352Arg
XM_005256400.3:c.652G>C	XP_005256457.1:p.Gly218Arg
XM_005256401.3:c.652G>C	XP_005256458.1:p.Gly218Arg
XM_005256402.3:c.652G>C	XP_005256459.1:p.Gly218Arg
XM_005256403.3:c.652G>C	XP_005256460.1:p.Gly218Arg
XM_005256404.3:c.652G>C	XP_005256461.1:p.Gly218Arg
XM_006722290.2:c.2257G>C	XP_006722353.1:p.Gly753Arg
XM_006722291.2:c.1042G>C	XP_006722354.1:p.Gly348Arg
XM_006722292.2:c.652G>C	XP_006722355.1:p.Gly218Arg
XM_011523589.1:c.1993G>C	XP_011521891.1:p.Gly665Arg
XM_011523590.1:c.1981G>C	XP_011521892.1:p.Gly661Arg
XM_011523591.1:c.1978G>C	XP_011521893.1:p.Gly660Arg
XM_011523592.1:c.1891G>C	XP_011521894.1:p.Gly631Arg
XM_011523593.1:c.1585G>C	XP_011521895.1:p.Gly529Arg
XM_011523594.1:c.1066G>C	XP_011521896.1:p.Gly356Arg
XM_011523595.1:c.1033G>C	XP_011521897.1:p.Gly345Arg
XM_011523596.1:c.*69G>C	XP_011521898.1:n.*69G>C
XM_011523597.1:c.799G>C	XP_011521899.1:p.Gly267Arg
XM_011523598.1:c.796G>C	XP_011521900.1:p.Gly266Arg
XM_011523599.1:c.790G>C	XP_011521901.1:p.Gly264Arg
XM_011523600.1:c.652G>C	XP_011521902.1:p.Gly218Arg
XR_430033.2:n.2446G>C
XM_005256396.4:c.2287G>C	XP_005256453.1:p.Gly763Arg
XM_005256399.5:c.1054G>C	XP_005256456.1:p.Gly352Arg
XM_005256404.4:c.652G>C	XP_005256461.1:p.Gly218Arg
XM_006722291.4:c.1042G>C	XP_006722354.1:p.Gly348Arg
XM_006722292.3:c.652G>C	XP_006722355.1:p.Gly218Arg
XM_011523589.2:c.1993G>C	XP_011521891.1:p.Gly665Arg
XM_011523591.2:c.1978G>C	XP_011521893.1:p.Gly660Arg
XM_011523593.2:c.1585G>C	XP_011521895.1:p.Gly529Arg
XM_011523594.2:c.1066G>C	XP_011521896.1:p.Gly356Arg
XM_011523595.3:c.1033G>C	XP_011521897.1:p.Gly345Arg
XM_011523597.2:c.799G>C	XP_011521899.1:p.Gly267Arg
XM_011523599.2:c.790G>C	XP_011521901.1:p.Gly264Arg
XM_011523600.3:c.652G>C	XP_011521902.1:p.Gly218Arg
XM_017024987.1:c.2149G>C	XP_016880476.1:p.Gly717Arg
XM_017024989.1:c.700G>C	XP_016880478.1:p.Gly234Arg
XM_017024990.2:c.652G>C	XP_016880479.1:p.Gly218Arg
XM_024450899.1:c.652G>C	XP_024306667.1:p.Gly218Arg
XM_024450900.1:c.652G>C	XP_024306668.1:p.Gly218Arg
XM_024450901.1:c.652G>C	XP_024306669.1:p.Gly218Arg
XM_024450902.1:c.652G>C	XP_024306670.1:p.Gly218Arg
XR_001752597.1:n.2446G>C
XR_001752598.1:n.2446G>C
XR_001752599.1:n.2446G>C
XR_001752600.1:n.2364G>C
NM_005993.5:c.2338G>C MANE Select	NP_005984.3:p.Gly780Arg