Canonical Allele Identifier: CA2172895277
Gene: TTBK2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.42777120C= , CM000677.2:g.42777120C= GRCh38
NC_000015.9:g.43069318C= , CM000677.1:g.43069318C= GRCh37
NC_000015.8:g.40856610C= NCBI36
NG_012664.1:g.148690G=

Transcript Alleles

HGVS Amino-acid change
ENST00000267890.11:c.1320G= MANE Select ENSP00000267890.6:p.Val440=
ENST00000267890.10:c.1320G= ENSP00000267890.6:p.Val440=
ENST00000567274.5:c.1215G= ENSP00000457489.1:p.Val405=
ENST00000567840.5:c.1320G= ENSP00000455734.1:p.Val440=
ENST00000622375.4:c.2535G= ENSP00000479984.1:p.Val845=
NM_173500.3:c.1320G= NP_775771.3:p.Val440=
XM_005254171.3:c.1338G= XP_005254228.1:p.Val446=
XM_005254173.3:c.1113G= XP_005254230.1:p.Val371=
XM_006720402.2:c.1305G= XP_006720465.1:p.Val435=
XM_006720403.2:c.1113G= XP_006720466.1:p.Val371=
XM_011521267.1:c.1113G= XP_011519569.1:p.Val371=
XM_011521268.1:c.1053G= XP_011519570.1:p.Val351=
XM_011521269.1:c.1041G= XP_011519571.1:p.Val347=
XM_005254171.5:c.1338G= XP_005254228.1:p.Val446=
XM_005254173.5:c.1113G= XP_005254230.1:p.Val371=
XM_006720402.4:c.1305G= XP_006720465.1:p.Val435=
XM_006720403.4:c.1113G= XP_006720466.1:p.Val371=
XM_017021950.2:c.1041G= XP_016877439.1:p.Val347=
XM_024449849.1:c.1320G= XP_024305617.1:p.Val440=
XM_024449850.1:c.1320G= XP_024305618.1:p.Val440=
XM_024449851.1:c.1113G= XP_024305619.1:p.Val371=
NM_173500.4:c.1320G= MANE Select NP_775771.3:p.Val440=