Canonical Allele Identifier: CA401633568

Gene: TBCD

Linked Data

• dbSNP Id: rs2061634548
• MyVariant Identifiers: chr17:g.80882901C>G (hg19) ; chr17:g.82925025C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.82925025C>G , CM000679.2:g.82925025C>G	GRCh38
NC_000017.10:g.80882901C>G , CM000679.1:g.80882901C>G	GRCh37
NC_000017.9:g.78476190C>G	NCBI36
NG_011721.1:g.177962C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000574886.2:n.1555C>G
ENST00000576677.6:n.1476C>G
ENST00000681983.1:n.2483C>G
ENST00000682099.1:n.1244C>G
ENST00000682213.1:c.*318C>G	ENSP00000508166.1:n.*318C>G
ENST00000682315.1:c.661C>G	ENSP00000507232.1:p.Pro221Ala
ENST00000682479.1:c.2437C>G	ENSP00000508214.1:p.Pro813Ala
ENST00000682610.1:n.1587C>G
ENST00000682654.1:c.*318C>G	ENSP00000507412.1:n.*318C>G
ENST00000682722.1:c.2296C>G	ENSP00000508364.1:p.Pro766Ala
ENST00000683041.1:c.*318C>G	ENSP00000506994.1:n.*318C>G
ENST00000683184.1:c.*2000C>G	ENSP00000507757.1:n.*2000C>G
ENST00000683282.1:c.2263C>G	ENSP00000506913.1:p.Pro755Ala
ENST00000683444.1:c.*1924C>G	ENSP00000507553.1:n.*1924C>G
ENST00000683584.1:n.1170C>G
ENST00000683821.1:c.661C>G	ENSP00000507651.1:p.Pro221Ala
ENST00000683839.1:n.1801C>G
ENST00000684000.1:c.2431C>G	ENSP00000506795.1:p.Pro811Ala
ENST00000684188.1:c.2158C>G	ENSP00000507153.1:p.Pro720Ala
ENST00000684349.1:c.2533C>G	ENSP00000508067.1:p.Pro845Ala
ENST00000684361.1:c.2347C>G	ENSP00000507364.1:p.Pro783Ala
ENST00000684408.1:c.1990C>G	ENSP00000506837.1:p.Pro664Ala
ENST00000684429.1:c.2275C>G	ENSP00000507224.1:p.Pro759Ala
ENST00000684464.1:c.2440C>G	ENSP00000508333.1:p.Pro814Ala
ENST00000684544.1:c.2266C>G	ENSP00000507337.1:p.Pro756Ala
ENST00000684559.1:n.1102C>G
ENST00000684760.1:c.2614C>G	ENSP00000507696.1:p.Pro872Ala
ENST00000684776.1:c.*830C>G	ENSP00000507861.1:n.*830C>G
ENST00000355528.9:c.2347C>G MANE Select	ENSP00000347719.4:p.Pro783Ala
ENST00000355528.8:c.2347C>G	ENSP00000347719.4:p.Pro783Ala
ENST00000539345.6:c.2347C>G	ENSP00000440671.2:p.Pro783Ala
ENST00000571618.5:n.525C>G
ENST00000571796.5:n.1005C>G
ENST00000574422.1:c.661C>G	ENSP00000458599.1:p.Pro221Ala
ENST00000574818.5:n.405C>G
ENST00000574886.1:n.731C>G
ENST00000574975.5:c.724C>G	ENSP00000461680.1:p.Pro242Ala
ENST00000576760.5:c.661C>G	ENSP00000460949.1:p.Pro221Ala
NM_005993.4:c.2347C>G	NP_005984.3:p.Pro783Ala
XM_005256396.3:c.2296C>G	XP_005256453.1:p.Pro766Ala
XM_005256399.3:c.1063C>G	XP_005256456.1:p.Pro355Ala
XM_005256400.3:c.661C>G	XP_005256457.1:p.Pro221Ala
XM_005256401.3:c.661C>G	XP_005256458.1:p.Pro221Ala
XM_005256402.3:c.661C>G	XP_005256459.1:p.Pro221Ala
XM_005256403.3:c.661C>G	XP_005256460.1:p.Pro221Ala
XM_005256404.3:c.661C>G	XP_005256461.1:p.Pro221Ala
XM_006722290.2:c.2266C>G	XP_006722353.1:p.Pro756Ala
XM_006722291.2:c.1051C>G	XP_006722354.1:p.Pro351Ala
XM_006722292.2:c.661C>G	XP_006722355.1:p.Pro221Ala
XM_011523589.1:c.2002C>G	XP_011521891.1:p.Pro668Ala
XM_011523590.1:c.1990C>G	XP_011521892.1:p.Pro664Ala
XM_011523591.1:c.1987C>G	XP_011521893.1:p.Pro663Ala
XM_011523592.1:c.1900C>G	XP_011521894.1:p.Pro634Ala
XM_011523593.1:c.1594C>G	XP_011521895.1:p.Pro532Ala
XM_011523594.1:c.1075C>G	XP_011521896.1:p.Pro359Ala
XM_011523595.1:c.1042C>G	XP_011521897.1:p.Pro348Ala
XM_011523596.1:c.*78C>G	XP_011521898.1:n.*78C>G
XM_011523597.1:c.808C>G	XP_011521899.1:p.Pro270Ala
XM_011523598.1:c.805C>G	XP_011521900.1:p.Pro269Ala
XM_011523599.1:c.799C>G	XP_011521901.1:p.Pro267Ala
XM_011523600.1:c.661C>G	XP_011521902.1:p.Pro221Ala
XR_430033.2:n.2455C>G
XM_005256396.4:c.2296C>G	XP_005256453.1:p.Pro766Ala
XM_005256399.5:c.1063C>G	XP_005256456.1:p.Pro355Ala
XM_005256404.4:c.661C>G	XP_005256461.1:p.Pro221Ala
XM_006722291.4:c.1051C>G	XP_006722354.1:p.Pro351Ala
XM_006722292.3:c.661C>G	XP_006722355.1:p.Pro221Ala
XM_011523589.2:c.2002C>G	XP_011521891.1:p.Pro668Ala
XM_011523591.2:c.1987C>G	XP_011521893.1:p.Pro663Ala
XM_011523593.2:c.1594C>G	XP_011521895.1:p.Pro532Ala
XM_011523594.2:c.1075C>G	XP_011521896.1:p.Pro359Ala
XM_011523595.3:c.1042C>G	XP_011521897.1:p.Pro348Ala
XM_011523597.2:c.808C>G	XP_011521899.1:p.Pro270Ala
XM_011523599.2:c.799C>G	XP_011521901.1:p.Pro267Ala
XM_011523600.3:c.661C>G	XP_011521902.1:p.Pro221Ala
XM_017024987.1:c.2158C>G	XP_016880476.1:p.Pro720Ala
XM_017024989.1:c.709C>G	XP_016880478.1:p.Pro237Ala
XM_017024990.2:c.661C>G	XP_016880479.1:p.Pro221Ala
XM_024450899.1:c.661C>G	XP_024306667.1:p.Pro221Ala
XM_024450900.1:c.661C>G	XP_024306668.1:p.Pro221Ala
XM_024450901.1:c.661C>G	XP_024306669.1:p.Pro221Ala
XM_024450902.1:c.661C>G	XP_024306670.1:p.Pro221Ala
XR_001752597.1:n.2455C>G
XR_001752598.1:n.2455C>G
XR_001752599.1:n.2455C>G
XR_001752600.1:n.2373C>G
NM_005993.5:c.2347C>G MANE Select	NP_005984.3:p.Pro783Ala