Canonical Allele Identifier: CA2172895134

Gene: TTBK2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42777024T= , CM000677.2:g.42777024T=	GRCh38
NC_000015.9:g.43069222T= , CM000677.1:g.43069222T=	GRCh37
NC_000015.8:g.40856514T=	NCBI36
NG_012664.1:g.148786A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000267890.11:c.1409+7A= MANE Select	ENSP00000267890.6:n.1409+7A=
ENST00000267890.10:c.1409+7A=	ENSP00000267890.6:n.1409+7A=
ENST00000567274.5:c.1311A=	ENSP00000457489.1:p.Lys437=
ENST00000567840.5:c.1416A=	ENSP00000455734.1:p.Lys472=
ENST00000622375.4:c.2624+7A=	ENSP00000479984.1:n.2624+7A=
NM_173500.3:c.1409+7A=	NP_775771.3:n.1409+7A=
XM_005254171.3:c.1427+7A=	XP_005254228.1:n.1427+7A=
XM_005254173.3:c.1202+7A=	XP_005254230.1:n.1202+7A=
XM_006720402.2:c.1394+7A=	XP_006720465.1:n.1394+7A=
XM_006720403.2:c.1202+7A=	XP_006720466.1:n.1202+7A=
XM_011521267.1:c.1202+7A=	XP_011519569.1:n.1202+7A=
XM_011521268.1:c.1142+7A=	XP_011519570.1:n.1142+7A=
XM_011521269.1:c.1130+7A=	XP_011519571.1:n.1130+7A=
XM_005254171.5:c.1427+7A=	XP_005254228.1:n.1427+7A=
XM_005254173.5:c.1202+7A=	XP_005254230.1:n.1202+7A=
XM_006720402.4:c.1394+7A=	XP_006720465.1:n.1394+7A=
XM_006720403.4:c.1202+7A=	XP_006720466.1:n.1202+7A=
XM_017021950.2:c.1130+7A=	XP_016877439.1:n.1130+7A=
XM_024449849.1:c.1409+7A=	XP_024305617.1:n.1409+7A=
XM_024449850.1:c.1409+7A=	XP_024305618.1:n.1409+7A=
XM_024449851.1:c.1202+7A=	XP_024305619.1:n.1202+7A=
NM_173500.4:c.1409+7A= MANE Select	NP_775771.3:n.1409+7A=