Canonical Allele Identifier: CA392015354

Gene: TTBK2

Linked Data

• MyVariant Identifiers: chr15:g.43069313T>C (hg19) ; chr15:g.42777115T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42777115T>C , CM000677.2:g.42777115T>C	GRCh38
NC_000015.9:g.43069313T>C , CM000677.1:g.43069313T>C	GRCh37
NC_000015.8:g.40856605T>C	NCBI36
NG_012664.1:g.148695A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000267890.11:c.1325A>G MANE Select	ENSP00000267890.6:p.Lys442Arg
ENST00000267890.10:c.1325A>G	ENSP00000267890.6:p.Lys442Arg
ENST00000567274.5:c.1220A>G	ENSP00000457489.1:p.Lys407Arg
ENST00000567840.5:c.1325A>G	ENSP00000455734.1:p.Lys442Arg
ENST00000622375.4:c.2540A>G	ENSP00000479984.1:p.Lys847Arg
NM_173500.3:c.1325A>G	NP_775771.3:p.Lys442Arg
XM_005254171.3:c.1343A>G	XP_005254228.1:p.Lys448Arg
XM_005254173.3:c.1118A>G	XP_005254230.1:p.Lys373Arg
XM_006720402.2:c.1310A>G	XP_006720465.1:p.Lys437Arg
XM_006720403.2:c.1118A>G	XP_006720466.1:p.Lys373Arg
XM_011521267.1:c.1118A>G	XP_011519569.1:p.Lys373Arg
XM_011521268.1:c.1058A>G	XP_011519570.1:p.Lys353Arg
XM_011521269.1:c.1046A>G	XP_011519571.1:p.Lys349Arg
XM_005254171.5:c.1343A>G	XP_005254228.1:p.Lys448Arg
XM_005254173.5:c.1118A>G	XP_005254230.1:p.Lys373Arg
XM_006720402.4:c.1310A>G	XP_006720465.1:p.Lys437Arg
XM_006720403.4:c.1118A>G	XP_006720466.1:p.Lys373Arg
XM_017021950.2:c.1046A>G	XP_016877439.1:p.Lys349Arg
XM_024449849.1:c.1325A>G	XP_024305617.1:p.Lys442Arg
XM_024449850.1:c.1325A>G	XP_024305618.1:p.Lys442Arg
XM_024449851.1:c.1118A>G	XP_024305619.1:p.Lys373Arg
NM_173500.4:c.1325A>G MANE Select	NP_775771.3:p.Lys442Arg