Canonical Allele Identifier: CA401633262

Gene: TBCD

Linked Data

• gnomAD v4: 17-82924944-C-A
• MyVariant Identifiers: chr17:g.80882820C>A (hg19) ; chr17:g.82924944C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82924944C>A , CM000679.2:g.82924944C>A	GRCh38
NC_000017.10:g.80882820C>A , CM000679.1:g.80882820C>A	GRCh37
NC_000017.9:g.78476109C>A	NCBI36
NG_011721.1:g.177881C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1474C>A
ENST00000576677.6:n.1395C>A
ENST00000681983.1:n.2402C>A
ENST00000682099.1:n.1163C>A
ENST00000682213.1:c.*237C>A	ENSP00000508166.1:n.*237C>A
ENST00000682315.1:c.580C>A	ENSP00000507232.1:p.Leu194Met
ENST00000682479.1:c.2356C>A	ENSP00000508214.1:p.Leu786Met
ENST00000682610.1:n.1506C>A
ENST00000682654.1:c.*237C>A	ENSP00000507412.1:n.*237C>A
ENST00000682722.1:c.2215C>A	ENSP00000508364.1:p.Leu739Met
ENST00000683041.1:c.*237C>A	ENSP00000506994.1:n.*237C>A
ENST00000683184.1:c.*1919C>A	ENSP00000507757.1:n.*1919C>A
ENST00000683282.1:c.2182C>A	ENSP00000506913.1:p.Leu728Met
ENST00000683444.1:c.*1843C>A	ENSP00000507553.1:n.*1843C>A
ENST00000683584.1:n.1089C>A
ENST00000683821.1:c.580C>A	ENSP00000507651.1:p.Leu194Met
ENST00000683839.1:n.1720C>A
ENST00000684000.1:c.2350C>A	ENSP00000506795.1:p.Leu784Met
ENST00000684188.1:c.2077C>A	ENSP00000507153.1:p.Leu693Met
ENST00000684349.1:c.2452C>A	ENSP00000508067.1:p.Leu818Met
ENST00000684361.1:c.2266C>A	ENSP00000507364.1:p.Leu756Met
ENST00000684408.1:c.1909C>A	ENSP00000506837.1:p.Leu637Met
ENST00000684429.1:c.2194C>A	ENSP00000507224.1:p.Leu732Met
ENST00000684464.1:c.2359C>A	ENSP00000508333.1:p.Leu787Met
ENST00000684544.1:c.2185C>A	ENSP00000507337.1:p.Leu729Met
ENST00000684559.1:n.1021C>A
ENST00000684760.1:c.2533C>A	ENSP00000507696.1:p.Leu845Met
ENST00000684776.1:c.*749C>A	ENSP00000507861.1:n.*749C>A
ENST00000355528.9:c.2266C>A MANE Select	ENSP00000347719.4:p.Leu756Met
ENST00000355528.8:c.2266C>A	ENSP00000347719.4:p.Leu756Met
ENST00000539345.6:c.2266C>A	ENSP00000440671.2:p.Leu756Met
ENST00000571618.5:n.444C>A
ENST00000571796.5:n.924C>A
ENST00000574422.1:c.580C>A	ENSP00000458599.1:p.Leu194Met
ENST00000574818.5:n.324C>A
ENST00000574886.1:n.650C>A
ENST00000574975.5:c.643C>A	ENSP00000461680.1:p.Leu215Met
ENST00000576760.5:c.580C>A	ENSP00000460949.1:p.Leu194Met
NM_005993.4:c.2266C>A	NP_005984.3:p.Leu756Met
XM_005256396.3:c.2215C>A	XP_005256453.1:p.Leu739Met
XM_005256399.3:c.982C>A	XP_005256456.1:p.Leu328Met
XM_005256400.3:c.580C>A	XP_005256457.1:p.Leu194Met
XM_005256401.3:c.580C>A	XP_005256458.1:p.Leu194Met
XM_005256402.3:c.580C>A	XP_005256459.1:p.Leu194Met
XM_005256403.3:c.580C>A	XP_005256460.1:p.Leu194Met
XM_005256404.3:c.580C>A	XP_005256461.1:p.Leu194Met
XM_006722290.2:c.2185C>A	XP_006722353.1:p.Leu729Met
XM_006722291.2:c.970C>A	XP_006722354.1:p.Leu324Met
XM_006722292.2:c.580C>A	XP_006722355.1:p.Leu194Met
XM_011523589.1:c.1921C>A	XP_011521891.1:p.Leu641Met
XM_011523590.1:c.1909C>A	XP_011521892.1:p.Leu637Met
XM_011523591.1:c.1906C>A	XP_011521893.1:p.Leu636Met
XM_011523592.1:c.1819C>A	XP_011521894.1:p.Leu607Met
XM_011523593.1:c.1513C>A	XP_011521895.1:p.Leu505Met
XM_011523594.1:c.994C>A	XP_011521896.1:p.Leu332Met
XM_011523595.1:c.961C>A	XP_011521897.1:p.Leu321Met
XM_011523596.1:c.2184C>A	XP_011521898.1:p.Ser728Arg
XM_011523597.1:c.727C>A	XP_011521899.1:p.Leu243Met
XM_011523598.1:c.724C>A	XP_011521900.1:p.Leu242Met
XM_011523599.1:c.718C>A	XP_011521901.1:p.Leu240Met
XM_011523600.1:c.580C>A	XP_011521902.1:p.Leu194Met
XR_430033.2:n.2374C>A
XM_005256396.4:c.2215C>A	XP_005256453.1:p.Leu739Met
XM_005256399.5:c.982C>A	XP_005256456.1:p.Leu328Met
XM_005256404.4:c.580C>A	XP_005256461.1:p.Leu194Met
XM_006722291.4:c.970C>A	XP_006722354.1:p.Leu324Met
XM_006722292.3:c.580C>A	XP_006722355.1:p.Leu194Met
XM_011523589.2:c.1921C>A	XP_011521891.1:p.Leu641Met
XM_011523591.2:c.1906C>A	XP_011521893.1:p.Leu636Met
XM_011523593.2:c.1513C>A	XP_011521895.1:p.Leu505Met
XM_011523594.2:c.994C>A	XP_011521896.1:p.Leu332Met
XM_011523595.3:c.961C>A	XP_011521897.1:p.Leu321Met
XM_011523597.2:c.727C>A	XP_011521899.1:p.Leu243Met
XM_011523599.2:c.718C>A	XP_011521901.1:p.Leu240Met
XM_011523600.3:c.580C>A	XP_011521902.1:p.Leu194Met
XM_017024987.1:c.2077C>A	XP_016880476.1:p.Leu693Met
XM_017024989.1:c.628C>A	XP_016880478.1:p.Leu210Met
XM_017024990.2:c.580C>A	XP_016880479.1:p.Leu194Met
XM_024450899.1:c.580C>A	XP_024306667.1:p.Leu194Met
XM_024450900.1:c.580C>A	XP_024306668.1:p.Leu194Met
XM_024450901.1:c.580C>A	XP_024306669.1:p.Leu194Met
XM_024450902.1:c.580C>A	XP_024306670.1:p.Leu194Met
XR_001752597.1:n.2374C>A
XR_001752598.1:n.2374C>A
XR_001752599.1:n.2374C>A
XR_001752600.1:n.2292C>A
NM_005993.5:c.2266C>A MANE Select	NP_005984.3:p.Leu756Met