Canonical Allele Identifier: CA489893004

Gene: TTBK2

Linked Data

• MyVariant Identifiers: chr15:g.43069366A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42777168A>T , CM000677.2:g.42777168A>T	GRCh38
NC_000015.9:g.43069366A>T , CM000677.1:g.43069366A>T	GRCh37
NC_000015.8:g.40856658A>T	NCBI36
NG_012664.1:g.148642T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000267890.11:c.1272T>A MANE Select	ENSP00000267890.6:p.Ile424=
ENST00000267890.10:c.1272T>A	ENSP00000267890.6:p.Ile424=
ENST00000567274.5:c.1167T>A	ENSP00000457489.1:p.Ile389=
ENST00000567840.5:c.1272T>A	ENSP00000455734.1:p.Ile424=
ENST00000622375.4:c.2487T>A	ENSP00000479984.1:p.Ile829=
NM_173500.3:c.1272T>A	NP_775771.3:p.Ile424=
XM_005254171.3:c.1290T>A	XP_005254228.1:p.Ile430=
XM_005254173.3:c.1065T>A	XP_005254230.1:p.Ile355=
XM_006720402.2:c.1257T>A	XP_006720465.1:p.Ile419=
XM_006720403.2:c.1065T>A	XP_006720466.1:p.Ile355=
XM_011521267.1:c.1065T>A	XP_011519569.1:p.Ile355=
XM_011521268.1:c.1005T>A	XP_011519570.1:p.Ile335=
XM_011521269.1:c.993T>A	XP_011519571.1:p.Ile331=
XM_005254171.5:c.1290T>A	XP_005254228.1:p.Ile430=
XM_005254173.5:c.1065T>A	XP_005254230.1:p.Ile355=
XM_006720402.4:c.1257T>A	XP_006720465.1:p.Ile419=
XM_006720403.4:c.1065T>A	XP_006720466.1:p.Ile355=
XM_017021950.2:c.993T>A	XP_016877439.1:p.Ile331=
XM_024449849.1:c.1272T>A	XP_024305617.1:p.Ile424=
XM_024449850.1:c.1272T>A	XP_024305618.1:p.Ile424=
XM_024449851.1:c.1065T>A	XP_024305619.1:p.Ile355=
NM_173500.4:c.1272T>A MANE Select	NP_775771.3:p.Ile424=