Canonical Allele Identifier: CA392014490

Gene: TTBK2

Linked Data

• MyVariant Identifiers: chr15:g.43069214T>G (hg19) ; chr15:g.42777016T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42777016T>G , CM000677.2:g.42777016T>G	GRCh38
NC_000015.9:g.43069214T>G , CM000677.1:g.43069214T>G	GRCh37
NC_000015.8:g.40856506T>G	NCBI36
NG_012664.1:g.148794A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000267890.11:c.1409+15A>C MANE Select	ENSP00000267890.6:n.1409+15A>C
ENST00000267890.10:c.1409+15A>C	ENSP00000267890.6:n.1409+15A>C
ENST00000567274.5:c.1319A>C	ENSP00000457489.1:p.Tyr440Ser
ENST00000567840.5:c.1424A>C	ENSP00000455734.1:p.Tyr475Ser
ENST00000622375.4:c.2624+15A>C	ENSP00000479984.1:n.2624+15A>C
NM_173500.3:c.1409+15A>C	NP_775771.3:n.1409+15A>C
XM_005254171.3:c.1427+15A>C	XP_005254228.1:n.1427+15A>C
XM_005254173.3:c.1202+15A>C	XP_005254230.1:n.1202+15A>C
XM_006720402.2:c.1394+15A>C	XP_006720465.1:n.1394+15A>C
XM_006720403.2:c.1202+15A>C	XP_006720466.1:n.1202+15A>C
XM_011521267.1:c.1202+15A>C	XP_011519569.1:n.1202+15A>C
XM_011521268.1:c.1142+15A>C	XP_011519570.1:n.1142+15A>C
XM_011521269.1:c.1130+15A>C	XP_011519571.1:n.1130+15A>C
XM_005254171.5:c.1427+15A>C	XP_005254228.1:n.1427+15A>C
XM_005254173.5:c.1202+15A>C	XP_005254230.1:n.1202+15A>C
XM_006720402.4:c.1394+15A>C	XP_006720465.1:n.1394+15A>C
XM_006720403.4:c.1202+15A>C	XP_006720466.1:n.1202+15A>C
XM_017021950.2:c.1130+15A>C	XP_016877439.1:n.1130+15A>C
XM_024449849.1:c.1409+15A>C	XP_024305617.1:n.1409+15A>C
XM_024449850.1:c.1409+15A>C	XP_024305618.1:n.1409+15A>C
XM_024449851.1:c.1202+15A>C	XP_024305619.1:n.1202+15A>C
NM_173500.4:c.1409+15A>C MANE Select	NP_775771.3:n.1409+15A>C