Canonical Allele Identifier: CA401633617

Gene: TBCD

Linked Data

• dbSNP Id: rs1254622271
• gnomAD v4: 17-82925037-C-A
• MyVariant Identifiers: chr17:g.80882913C>A (hg19) ; chr17:g.82925037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82925037C>A , CM000679.2:g.82925037C>A	GRCh38
NC_000017.10:g.80882913C>A , CM000679.1:g.80882913C>A	GRCh37
NC_000017.9:g.78476202C>A	NCBI36
NG_011721.1:g.177974C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1567C>A
ENST00000576677.6:n.1488C>A
ENST00000681983.1:n.2495C>A
ENST00000682099.1:n.1256C>A
ENST00000682213.1:c.*330C>A	ENSP00000508166.1:n.*330C>A
ENST00000682315.1:c.673C>A	ENSP00000507232.1:p.Leu225Met
ENST00000682479.1:c.2449C>A	ENSP00000508214.1:p.Leu817Met
ENST00000682610.1:n.1599C>A
ENST00000682654.1:c.*330C>A	ENSP00000507412.1:n.*330C>A
ENST00000682722.1:c.2308C>A	ENSP00000508364.1:p.Leu770Met
ENST00000683041.1:c.*330C>A	ENSP00000506994.1:n.*330C>A
ENST00000683184.1:c.*2012C>A	ENSP00000507757.1:n.*2012C>A
ENST00000683282.1:c.2275C>A	ENSP00000506913.1:p.Leu759Met
ENST00000683444.1:c.*1936C>A	ENSP00000507553.1:n.*1936C>A
ENST00000683584.1:n.1182C>A
ENST00000683821.1:c.673C>A	ENSP00000507651.1:p.Leu225Met
ENST00000683839.1:n.1813C>A
ENST00000684000.1:c.2443C>A	ENSP00000506795.1:p.Leu815Met
ENST00000684188.1:c.2170C>A	ENSP00000507153.1:p.Leu724Met
ENST00000684349.1:c.2545C>A	ENSP00000508067.1:p.Leu849Met
ENST00000684361.1:c.2359C>A	ENSP00000507364.1:p.Leu787Met
ENST00000684408.1:c.2002C>A	ENSP00000506837.1:p.Leu668Met
ENST00000684429.1:c.2287C>A	ENSP00000507224.1:p.Leu763Met
ENST00000684464.1:c.2452C>A	ENSP00000508333.1:p.Leu818Met
ENST00000684544.1:c.2278C>A	ENSP00000507337.1:p.Leu760Met
ENST00000684559.1:n.1114C>A
ENST00000684760.1:c.2626C>A	ENSP00000507696.1:p.Leu876Met
ENST00000684776.1:c.*842C>A	ENSP00000507861.1:n.*842C>A
ENST00000355528.9:c.2359C>A MANE Select	ENSP00000347719.4:p.Leu787Met
ENST00000355528.8:c.2359C>A	ENSP00000347719.4:p.Leu787Met
ENST00000539345.6:c.2359C>A	ENSP00000440671.2:p.Leu787Met
ENST00000571618.5:n.537C>A
ENST00000571796.5:n.1017C>A
ENST00000574422.1:c.673C>A	ENSP00000458599.1:p.Leu225Met
ENST00000574818.5:n.417C>A
ENST00000574886.1:n.743C>A
ENST00000574975.5:c.736C>A	ENSP00000461680.1:p.Leu246Met
ENST00000576760.5:c.673C>A	ENSP00000460949.1:p.Leu225Met
NM_005993.4:c.2359C>A	NP_005984.3:p.Leu787Met
XM_005256396.3:c.2308C>A	XP_005256453.1:p.Leu770Met
XM_005256399.3:c.1075C>A	XP_005256456.1:p.Leu359Met
XM_005256400.3:c.673C>A	XP_005256457.1:p.Leu225Met
XM_005256401.3:c.673C>A	XP_005256458.1:p.Leu225Met
XM_005256402.3:c.673C>A	XP_005256459.1:p.Leu225Met
XM_005256403.3:c.673C>A	XP_005256460.1:p.Leu225Met
XM_005256404.3:c.673C>A	XP_005256461.1:p.Leu225Met
XM_006722290.2:c.2278C>A	XP_006722353.1:p.Leu760Met
XM_006722291.2:c.1063C>A	XP_006722354.1:p.Leu355Met
XM_006722292.2:c.673C>A	XP_006722355.1:p.Leu225Met
XM_011523589.1:c.2014C>A	XP_011521891.1:p.Leu672Met
XM_011523590.1:c.2002C>A	XP_011521892.1:p.Leu668Met
XM_011523591.1:c.1999C>A	XP_011521893.1:p.Leu667Met
XM_011523592.1:c.1912C>A	XP_011521894.1:p.Leu638Met
XM_011523593.1:c.1606C>A	XP_011521895.1:p.Leu536Met
XM_011523594.1:c.1087C>A	XP_011521896.1:p.Leu363Met
XM_011523595.1:c.1054C>A	XP_011521897.1:p.Leu352Met
XM_011523597.1:c.820C>A	XP_011521899.1:p.Leu274Met
XM_011523598.1:c.817C>A	XP_011521900.1:p.Leu273Met
XM_011523599.1:c.811C>A	XP_011521901.1:p.Leu271Met
XM_011523600.1:c.673C>A	XP_011521902.1:p.Leu225Met
XR_430033.2:n.2467C>A
XM_005256396.4:c.2308C>A	XP_005256453.1:p.Leu770Met
XM_005256399.5:c.1075C>A	XP_005256456.1:p.Leu359Met
XM_005256404.4:c.673C>A	XP_005256461.1:p.Leu225Met
XM_006722291.4:c.1063C>A	XP_006722354.1:p.Leu355Met
XM_006722292.3:c.673C>A	XP_006722355.1:p.Leu225Met
XM_011523589.2:c.2014C>A	XP_011521891.1:p.Leu672Met
XM_011523591.2:c.1999C>A	XP_011521893.1:p.Leu667Met
XM_011523593.2:c.1606C>A	XP_011521895.1:p.Leu536Met
XM_011523594.2:c.1087C>A	XP_011521896.1:p.Leu363Met
XM_011523595.3:c.1054C>A	XP_011521897.1:p.Leu352Met
XM_011523597.2:c.820C>A	XP_011521899.1:p.Leu274Met
XM_011523599.2:c.811C>A	XP_011521901.1:p.Leu271Met
XM_011523600.3:c.673C>A	XP_011521902.1:p.Leu225Met
XM_017024987.1:c.2170C>A	XP_016880476.1:p.Leu724Met
XM_017024989.1:c.721C>A	XP_016880478.1:p.Leu241Met
XM_017024990.2:c.673C>A	XP_016880479.1:p.Leu225Met
XM_024450899.1:c.673C>A	XP_024306667.1:p.Leu225Met
XM_024450900.1:c.673C>A	XP_024306668.1:p.Leu225Met
XM_024450901.1:c.673C>A	XP_024306669.1:p.Leu225Met
XM_024450902.1:c.673C>A	XP_024306670.1:p.Leu225Met
XR_001752597.1:n.2467C>A
XR_001752598.1:n.2467C>A
XR_001752599.1:n.2467C>A
XR_001752600.1:n.2385C>A
NM_005993.5:c.2359C>A MANE Select	NP_005984.3:p.Leu787Met