Canonical Allele Identifier: CA401633456

Gene: TBCD

Linked Data

• MyVariant Identifiers: chr17:g.80882874G>C (hg19) ; chr17:g.82924998G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82924998G>C , CM000679.2:g.82924998G>C	GRCh38
NC_000017.10:g.80882874G>C , CM000679.1:g.80882874G>C	GRCh37
NC_000017.9:g.78476163G>C	NCBI36
NG_011721.1:g.177935G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1528G>C
ENST00000576677.6:n.1449G>C
ENST00000681983.1:n.2456G>C
ENST00000682099.1:n.1217G>C
ENST00000682213.1:c.*291G>C	ENSP00000508166.1:n.*291G>C
ENST00000682315.1:c.634G>C	ENSP00000507232.1:p.Gly212Arg
ENST00000682479.1:c.2410G>C	ENSP00000508214.1:p.Gly804Arg
ENST00000682610.1:n.1560G>C
ENST00000682654.1:c.*291G>C	ENSP00000507412.1:n.*291G>C
ENST00000682722.1:c.2269G>C	ENSP00000508364.1:p.Gly757Arg
ENST00000683041.1:c.*291G>C	ENSP00000506994.1:n.*291G>C
ENST00000683184.1:c.*1973G>C	ENSP00000507757.1:n.*1973G>C
ENST00000683282.1:c.2236G>C	ENSP00000506913.1:p.Gly746Arg
ENST00000683444.1:c.*1897G>C	ENSP00000507553.1:n.*1897G>C
ENST00000683584.1:n.1143G>C
ENST00000683821.1:c.634G>C	ENSP00000507651.1:p.Gly212Arg
ENST00000683839.1:n.1774G>C
ENST00000684000.1:c.2404G>C	ENSP00000506795.1:p.Gly802Arg
ENST00000684188.1:c.2131G>C	ENSP00000507153.1:p.Gly711Arg
ENST00000684349.1:c.2506G>C	ENSP00000508067.1:p.Gly836Arg
ENST00000684361.1:c.2320G>C	ENSP00000507364.1:p.Gly774Arg
ENST00000684408.1:c.1963G>C	ENSP00000506837.1:p.Gly655Arg
ENST00000684429.1:c.2248G>C	ENSP00000507224.1:p.Gly750Arg
ENST00000684464.1:c.2413G>C	ENSP00000508333.1:p.Gly805Arg
ENST00000684544.1:c.2239G>C	ENSP00000507337.1:p.Gly747Arg
ENST00000684559.1:n.1075G>C
ENST00000684760.1:c.2587G>C	ENSP00000507696.1:p.Gly863Arg
ENST00000684776.1:c.*803G>C	ENSP00000507861.1:n.*803G>C
ENST00000355528.9:c.2320G>C MANE Select	ENSP00000347719.4:p.Gly774Arg
ENST00000355528.8:c.2320G>C	ENSP00000347719.4:p.Gly774Arg
ENST00000539345.6:c.2320G>C	ENSP00000440671.2:p.Gly774Arg
ENST00000571618.5:n.498G>C
ENST00000571796.5:n.978G>C
ENST00000574422.1:c.634G>C	ENSP00000458599.1:p.Gly212Arg
ENST00000574818.5:n.378G>C
ENST00000574886.1:n.704G>C
ENST00000574975.5:c.697G>C	ENSP00000461680.1:p.Gly233Arg
ENST00000576760.5:c.634G>C	ENSP00000460949.1:p.Gly212Arg
NM_005993.4:c.2320G>C	NP_005984.3:p.Gly774Arg
XM_005256396.3:c.2269G>C	XP_005256453.1:p.Gly757Arg
XM_005256399.3:c.1036G>C	XP_005256456.1:p.Gly346Arg
XM_005256400.3:c.634G>C	XP_005256457.1:p.Gly212Arg
XM_005256401.3:c.634G>C	XP_005256458.1:p.Gly212Arg
XM_005256402.3:c.634G>C	XP_005256459.1:p.Gly212Arg
XM_005256403.3:c.634G>C	XP_005256460.1:p.Gly212Arg
XM_005256404.3:c.634G>C	XP_005256461.1:p.Gly212Arg
XM_006722290.2:c.2239G>C	XP_006722353.1:p.Gly747Arg
XM_006722291.2:c.1024G>C	XP_006722354.1:p.Gly342Arg
XM_006722292.2:c.634G>C	XP_006722355.1:p.Gly212Arg
XM_011523589.1:c.1975G>C	XP_011521891.1:p.Gly659Arg
XM_011523590.1:c.1963G>C	XP_011521892.1:p.Gly655Arg
XM_011523591.1:c.1960G>C	XP_011521893.1:p.Gly654Arg
XM_011523592.1:c.1873G>C	XP_011521894.1:p.Gly625Arg
XM_011523593.1:c.1567G>C	XP_011521895.1:p.Gly523Arg
XM_011523594.1:c.1048G>C	XP_011521896.1:p.Gly350Arg
XM_011523595.1:c.1015G>C	XP_011521897.1:p.Gly339Arg
XM_011523596.1:c.*51G>C	XP_011521898.1:n.*51G>C
XM_011523597.1:c.781G>C	XP_011521899.1:p.Gly261Arg
XM_011523598.1:c.778G>C	XP_011521900.1:p.Gly260Arg
XM_011523599.1:c.772G>C	XP_011521901.1:p.Gly258Arg
XM_011523600.1:c.634G>C	XP_011521902.1:p.Gly212Arg
XR_430033.2:n.2428G>C
XM_005256396.4:c.2269G>C	XP_005256453.1:p.Gly757Arg
XM_005256399.5:c.1036G>C	XP_005256456.1:p.Gly346Arg
XM_005256404.4:c.634G>C	XP_005256461.1:p.Gly212Arg
XM_006722291.4:c.1024G>C	XP_006722354.1:p.Gly342Arg
XM_006722292.3:c.634G>C	XP_006722355.1:p.Gly212Arg
XM_011523589.2:c.1975G>C	XP_011521891.1:p.Gly659Arg
XM_011523591.2:c.1960G>C	XP_011521893.1:p.Gly654Arg
XM_011523593.2:c.1567G>C	XP_011521895.1:p.Gly523Arg
XM_011523594.2:c.1048G>C	XP_011521896.1:p.Gly350Arg
XM_011523595.3:c.1015G>C	XP_011521897.1:p.Gly339Arg
XM_011523597.2:c.781G>C	XP_011521899.1:p.Gly261Arg
XM_011523599.2:c.772G>C	XP_011521901.1:p.Gly258Arg
XM_011523600.3:c.634G>C	XP_011521902.1:p.Gly212Arg
XM_017024987.1:c.2131G>C	XP_016880476.1:p.Gly711Arg
XM_017024989.1:c.682G>C	XP_016880478.1:p.Gly228Arg
XM_017024990.2:c.634G>C	XP_016880479.1:p.Gly212Arg
XM_024450899.1:c.634G>C	XP_024306667.1:p.Gly212Arg
XM_024450900.1:c.634G>C	XP_024306668.1:p.Gly212Arg
XM_024450901.1:c.634G>C	XP_024306669.1:p.Gly212Arg
XM_024450902.1:c.634G>C	XP_024306670.1:p.Gly212Arg
XR_001752597.1:n.2428G>C
XR_001752598.1:n.2428G>C
XR_001752599.1:n.2428G>C
XR_001752600.1:n.2346G>C
NM_005993.5:c.2320G>C MANE Select	NP_005984.3:p.Gly774Arg