Canonical Allele Identifier: CA3212163160

Gene: TTBK2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42777111T= , CM000677.2:g.42777111T=	GRCh38
NC_000015.9:g.43069309T= , CM000677.1:g.43069309T=	GRCh37
NC_000015.8:g.40856601T=	NCBI36
NG_012664.1:g.148699A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267890.11:c.1329A= MANE Select	ENSP00000267890.6:p.Leu443=
ENST00000267890.10:c.1329A=	ENSP00000267890.6:p.Leu443=
ENST00000567274.5:c.1224A=	ENSP00000457489.1:p.Leu408=
ENST00000567840.5:c.1329A=	ENSP00000455734.1:p.Leu443=
ENST00000622375.4:c.2544A=	ENSP00000479984.1:p.Leu848=
NM_173500.3:c.1329A=	NP_775771.3:p.Leu443=
XM_005254171.3:c.1347A=	XP_005254228.1:p.Leu449=
XM_005254173.3:c.1122A=	XP_005254230.1:p.Leu374=
XM_006720402.2:c.1314A=	XP_006720465.1:p.Leu438=
XM_006720403.2:c.1122A=	XP_006720466.1:p.Leu374=
XM_011521267.1:c.1122A=	XP_011519569.1:p.Leu374=
XM_011521268.1:c.1062A=	XP_011519570.1:p.Leu354=
XM_011521269.1:c.1050A=	XP_011519571.1:p.Leu350=
XM_005254171.5:c.1347A=	XP_005254228.1:p.Leu449=
XM_005254173.5:c.1122A=	XP_005254230.1:p.Leu374=
XM_006720402.4:c.1314A=	XP_006720465.1:p.Leu438=
XM_006720403.4:c.1122A=	XP_006720466.1:p.Leu374=
XM_017021950.2:c.1050A=	XP_016877439.1:p.Leu350=
XM_024449849.1:c.1329A=	XP_024305617.1:p.Leu443=
XM_024449850.1:c.1329A=	XP_024305618.1:p.Leu443=
XM_024449851.1:c.1122A=	XP_024305619.1:p.Leu374=
NM_173500.4:c.1329A= MANE Select	NP_775771.3:p.Leu443=