Canonical Allele Identifier: CA2279278210

Gene: TBCD

Linked Data

• dbSNP Id: rs573954205

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82925097G>C , CM000679.2:g.82925097G>C	GRCh38
NC_000017.10:g.80882973G>C , CM000679.1:g.80882973G>C	GRCh37
NC_000017.9:g.78476262G>C	NCBI36
NG_011721.1:g.178034G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1587+40G>C
ENST00000576677.6:n.1508+40G>C
ENST00000681983.1:n.2515+40G>C
ENST00000682099.1:n.1276+40G>C
ENST00000682213.1:c.*350+40G>C	ENSP00000508166.1:n.*350+40G>C
ENST00000682315.1:c.693+40G>C	ENSP00000507232.1:n.693+40G>C
ENST00000682479.1:c.2469+40G>C	ENSP00000508214.1:n.2469+40G>C
ENST00000682610.1:n.1619+40G>C
ENST00000682654.1:c.*350+40G>C	ENSP00000507412.1:n.*350+40G>C
ENST00000682722.1:c.2328+40G>C	ENSP00000508364.1:n.2328+40G>C
ENST00000683041.1:c.*350+40G>C	ENSP00000506994.1:n.*350+40G>C
ENST00000683184.1:c.*2032+40G>C	ENSP00000507757.1:n.*2032+40G>C
ENST00000683282.1:c.2295+40G>C	ENSP00000506913.1:n.2295+40G>C
ENST00000683444.1:c.*1956+40G>C	ENSP00000507553.1:n.*1956+40G>C
ENST00000683584.1:n.1202+40G>C
ENST00000683821.1:c.693+40G>C	ENSP00000507651.1:n.693+40G>C
ENST00000683839.1:n.1833+40G>C
ENST00000684000.1:c.2463+40G>C	ENSP00000506795.1:n.2463+40G>C
ENST00000684188.1:c.2190+40G>C	ENSP00000507153.1:n.2190+40G>C
ENST00000684349.1:c.2565+40G>C	ENSP00000508067.1:n.2565+40G>C
ENST00000684361.1:c.2379+40G>C	ENSP00000507364.1:n.2379+40G>C
ENST00000684408.1:c.2022+40G>C	ENSP00000506837.1:n.2022+40G>C
ENST00000684429.1:c.2307+40G>C	ENSP00000507224.1:n.2307+40G>C
ENST00000684464.1:c.2472+40G>C	ENSP00000508333.1:n.2472+40G>C
ENST00000684544.1:c.2298+40G>C	ENSP00000507337.1:n.2298+40G>C
ENST00000684559.1:n.1134+40G>C
ENST00000684760.1:c.2646+40G>C	ENSP00000507696.1:n.2646+40G>C
ENST00000684776.1:c.*862+40G>C	ENSP00000507861.1:n.*862+40G>C
ENST00000355528.9:c.2379+40G>C MANE Select	ENSP00000347719.4:n.2379+40G>C
ENST00000355528.8:c.2379+40G>C	ENSP00000347719.4:n.2379+40G>C
ENST00000539345.6:c.2379+40G>C	ENSP00000440671.2:n.2379+40G>C
ENST00000571618.5:n.557+40G>C
ENST00000571796.5:n.1037+40G>C
ENST00000574422.1:c.693+40G>C	ENSP00000458599.1:n.693+40G>C
ENST00000574818.5:n.437+40G>C
ENST00000574886.1:n.763+40G>C
ENST00000576760.5:c.693+40G>C	ENSP00000460949.1:n.693+40G>C
NM_005993.4:c.2379+40G>C	NP_005984.3:n.2379+40G>C
XM_005256396.3:c.2328+40G>C	XP_005256453.1:n.2328+40G>C
XM_005256399.3:c.1095+40G>C	XP_005256456.1:n.1095+40G>C
XM_005256400.3:c.693+40G>C	XP_005256457.1:n.693+40G>C
XM_005256401.3:c.693+40G>C	XP_005256458.1:n.693+40G>C
XM_005256402.3:c.693+40G>C	XP_005256459.1:n.693+40G>C
XM_005256403.3:c.693+40G>C	XP_005256460.1:n.693+40G>C
XM_005256404.3:c.693+40G>C	XP_005256461.1:n.693+40G>C
XM_006722290.2:c.2298+40G>C	XP_006722353.1:n.2298+40G>C
XM_006722291.2:c.1083+40G>C	XP_006722354.1:n.1083+40G>C
XM_006722292.2:c.693+40G>C	XP_006722355.1:n.693+40G>C
XM_011523589.1:c.2034+40G>C	XP_011521891.1:n.2034+40G>C
XM_011523590.1:c.2022+40G>C	XP_011521892.1:n.2022+40G>C
XM_011523591.1:c.2019+40G>C	XP_011521893.1:n.2019+40G>C
XM_011523592.1:c.1932+40G>C	XP_011521894.1:n.1932+40G>C
XM_011523593.1:c.1626+40G>C	XP_011521895.1:n.1626+40G>C
XM_011523594.1:c.1107+40G>C	XP_011521896.1:n.1107+40G>C
XM_011523595.1:c.1074+40G>C	XP_011521897.1:n.1074+40G>C
XM_011523597.1:c.840+40G>C	XP_011521899.1:n.840+40G>C
XM_011523598.1:c.837+40G>C	XP_011521900.1:n.837+40G>C
XM_011523599.1:c.831+40G>C	XP_011521901.1:n.831+40G>C
XM_011523600.1:c.693+40G>C	XP_011521902.1:n.693+40G>C
XR_430033.2:n.2487+40G>C
XM_005256396.4:c.2328+40G>C	XP_005256453.1:n.2328+40G>C
XM_005256399.5:c.1095+40G>C	XP_005256456.1:n.1095+40G>C
XM_005256404.4:c.693+40G>C	XP_005256461.1:n.693+40G>C
XM_006722291.4:c.1083+40G>C	XP_006722354.1:n.1083+40G>C
XM_006722292.3:c.693+40G>C	XP_006722355.1:n.693+40G>C
XM_011523589.2:c.2034+40G>C	XP_011521891.1:n.2034+40G>C
XM_011523591.2:c.2019+40G>C	XP_011521893.1:n.2019+40G>C
XM_011523593.2:c.1626+40G>C	XP_011521895.1:n.1626+40G>C
XM_011523594.2:c.1107+40G>C	XP_011521896.1:n.1107+40G>C
XM_011523595.3:c.1074+40G>C	XP_011521897.1:n.1074+40G>C
XM_011523597.2:c.840+40G>C	XP_011521899.1:n.840+40G>C
XM_011523599.2:c.831+40G>C	XP_011521901.1:n.831+40G>C
XM_011523600.3:c.693+40G>C	XP_011521902.1:n.693+40G>C
XM_017024987.1:c.2190+40G>C	XP_016880476.1:n.2190+40G>C
XM_017024989.1:c.741+40G>C	XP_016880478.1:n.741+40G>C
XM_017024990.2:c.693+40G>C	XP_016880479.1:n.693+40G>C
XM_024450899.1:c.693+40G>C	XP_024306667.1:n.693+40G>C
XM_024450900.1:c.693+40G>C	XP_024306668.1:n.693+40G>C
XM_024450901.1:c.693+40G>C	XP_024306669.1:n.693+40G>C
XM_024450902.1:c.693+40G>C	XP_024306670.1:n.693+40G>C
XR_001752597.1:n.2487+40G>C
XR_001752598.1:n.2487+40G>C
XR_001752599.1:n.2487+40G>C
XR_001752600.1:n.2405+40G>C
NM_005993.5:c.2379+40G>C MANE Select	NP_005984.3:n.2379+40G>C