Canonical Allele Identifier: CA401633496

Gene: TBCD

Linked Data

• MyVariant Identifiers: chr17:g.80882884T>A (hg19) ; chr17:g.82925008T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82925008T>A , CM000679.2:g.82925008T>A	GRCh38
NC_000017.10:g.80882884T>A , CM000679.1:g.80882884T>A	GRCh37
NC_000017.9:g.78476173T>A	NCBI36
NG_011721.1:g.177945T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1538T>A
ENST00000576677.6:n.1459T>A
ENST00000681983.1:n.2466T>A
ENST00000682099.1:n.1227T>A
ENST00000682213.1:c.*301T>A	ENSP00000508166.1:n.*301T>A
ENST00000682315.1:c.644T>A	ENSP00000507232.1:p.Leu215Ter
ENST00000682479.1:c.2420T>A	ENSP00000508214.1:p.Leu807Ter
ENST00000682610.1:n.1570T>A
ENST00000682654.1:c.*301T>A	ENSP00000507412.1:n.*301T>A
ENST00000682722.1:c.2279T>A	ENSP00000508364.1:p.Leu760Ter
ENST00000683041.1:c.*301T>A	ENSP00000506994.1:n.*301T>A
ENST00000683184.1:c.*1983T>A	ENSP00000507757.1:n.*1983T>A
ENST00000683282.1:c.2246T>A	ENSP00000506913.1:p.Leu749Ter
ENST00000683444.1:c.*1907T>A	ENSP00000507553.1:n.*1907T>A
ENST00000683584.1:n.1153T>A
ENST00000683821.1:c.644T>A	ENSP00000507651.1:p.Leu215Ter
ENST00000683839.1:n.1784T>A
ENST00000684000.1:c.2414T>A	ENSP00000506795.1:p.Leu805Ter
ENST00000684188.1:c.2141T>A	ENSP00000507153.1:p.Leu714Ter
ENST00000684349.1:c.2516T>A	ENSP00000508067.1:p.Leu839Ter
ENST00000684361.1:c.2330T>A	ENSP00000507364.1:p.Leu777Ter
ENST00000684408.1:c.1973T>A	ENSP00000506837.1:p.Leu658Ter
ENST00000684429.1:c.2258T>A	ENSP00000507224.1:p.Leu753Ter
ENST00000684464.1:c.2423T>A	ENSP00000508333.1:p.Leu808Ter
ENST00000684544.1:c.2249T>A	ENSP00000507337.1:p.Leu750Ter
ENST00000684559.1:n.1085T>A
ENST00000684760.1:c.2597T>A	ENSP00000507696.1:p.Leu866Ter
ENST00000684776.1:c.*813T>A	ENSP00000507861.1:n.*813T>A
ENST00000355528.9:c.2330T>A MANE Select	ENSP00000347719.4:p.Leu777Ter
ENST00000355528.8:c.2330T>A	ENSP00000347719.4:p.Leu777Ter
ENST00000539345.6:c.2330T>A	ENSP00000440671.2:p.Leu777Ter
ENST00000571618.5:n.508T>A
ENST00000571796.5:n.988T>A
ENST00000574422.1:c.644T>A	ENSP00000458599.1:p.Leu215Ter
ENST00000574818.5:n.388T>A
ENST00000574886.1:n.714T>A
ENST00000574975.5:c.707T>A	ENSP00000461680.1:p.Leu236Ter
ENST00000576760.5:c.644T>A	ENSP00000460949.1:p.Leu215Ter
NM_005993.4:c.2330T>A	NP_005984.3:p.Leu777Ter
XM_005256396.3:c.2279T>A	XP_005256453.1:p.Leu760Ter
XM_005256399.3:c.1046T>A	XP_005256456.1:p.Leu349Ter
XM_005256400.3:c.644T>A	XP_005256457.1:p.Leu215Ter
XM_005256401.3:c.644T>A	XP_005256458.1:p.Leu215Ter
XM_005256402.3:c.644T>A	XP_005256459.1:p.Leu215Ter
XM_005256403.3:c.644T>A	XP_005256460.1:p.Leu215Ter
XM_005256404.3:c.644T>A	XP_005256461.1:p.Leu215Ter
XM_006722290.2:c.2249T>A	XP_006722353.1:p.Leu750Ter
XM_006722291.2:c.1034T>A	XP_006722354.1:p.Leu345Ter
XM_006722292.2:c.644T>A	XP_006722355.1:p.Leu215Ter
XM_011523589.1:c.1985T>A	XP_011521891.1:p.Leu662Ter
XM_011523590.1:c.1973T>A	XP_011521892.1:p.Leu658Ter
XM_011523591.1:c.1970T>A	XP_011521893.1:p.Leu657Ter
XM_011523592.1:c.1883T>A	XP_011521894.1:p.Leu628Ter
XM_011523593.1:c.1577T>A	XP_011521895.1:p.Leu526Ter
XM_011523594.1:c.1058T>A	XP_011521896.1:p.Leu353Ter
XM_011523595.1:c.1025T>A	XP_011521897.1:p.Leu342Ter
XM_011523596.1:c.*61T>A	XP_011521898.1:n.*61T>A
XM_011523597.1:c.791T>A	XP_011521899.1:p.Leu264Ter
XM_011523598.1:c.788T>A	XP_011521900.1:p.Leu263Ter
XM_011523599.1:c.782T>A	XP_011521901.1:p.Leu261Ter
XM_011523600.1:c.644T>A	XP_011521902.1:p.Leu215Ter
XR_430033.2:n.2438T>A
XM_005256396.4:c.2279T>A	XP_005256453.1:p.Leu760Ter
XM_005256399.5:c.1046T>A	XP_005256456.1:p.Leu349Ter
XM_005256404.4:c.644T>A	XP_005256461.1:p.Leu215Ter
XM_006722291.4:c.1034T>A	XP_006722354.1:p.Leu345Ter
XM_006722292.3:c.644T>A	XP_006722355.1:p.Leu215Ter
XM_011523589.2:c.1985T>A	XP_011521891.1:p.Leu662Ter
XM_011523591.2:c.1970T>A	XP_011521893.1:p.Leu657Ter
XM_011523593.2:c.1577T>A	XP_011521895.1:p.Leu526Ter
XM_011523594.2:c.1058T>A	XP_011521896.1:p.Leu353Ter
XM_011523595.3:c.1025T>A	XP_011521897.1:p.Leu342Ter
XM_011523597.2:c.791T>A	XP_011521899.1:p.Leu264Ter
XM_011523599.2:c.782T>A	XP_011521901.1:p.Leu261Ter
XM_011523600.3:c.644T>A	XP_011521902.1:p.Leu215Ter
XM_017024987.1:c.2141T>A	XP_016880476.1:p.Leu714Ter
XM_017024989.1:c.692T>A	XP_016880478.1:p.Leu231Ter
XM_017024990.2:c.644T>A	XP_016880479.1:p.Leu215Ter
XM_024450899.1:c.644T>A	XP_024306667.1:p.Leu215Ter
XM_024450900.1:c.644T>A	XP_024306668.1:p.Leu215Ter
XM_024450901.1:c.644T>A	XP_024306669.1:p.Leu215Ter
XM_024450902.1:c.644T>A	XP_024306670.1:p.Leu215Ter
XR_001752597.1:n.2438T>A
XR_001752598.1:n.2438T>A
XR_001752599.1:n.2438T>A
XR_001752600.1:n.2356T>A
NM_005993.5:c.2330T>A MANE Select	NP_005984.3:p.Leu777Ter