Canonical Allele Identifier: CA1624430396
Gene: TTBK1 HGNC NCBI

Linked Data

dbSNP Id: rs2651206

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.43245739C>A , CM000668.2:g.43245739C>A GRCh38
NC_000006.11:g.43213477C>A , CM000668.1:g.43213477C>A GRCh37
NC_000006.10:g.43321455C>A NCBI36
NG_051244.1:g.7060C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000259750.9:c.-54-868C>A MANE Select ENSP00000259750.4:n.-54-868C>A
ENST00000259750.8:c.-54-868C>A ENSP00000259750.4:n.-54-868C>A
NM_032538.1:c.-54-868C>A NP_115927.1:n.-54-868C>A
XM_011514945.1:c.39+547C>A XP_011513247.1:n.39+547C>A
XM_011514946.1:c.39+547C>A XP_011513248.1:n.39+547C>A
XM_011514947.1:c.-54-868C>A XP_011513249.1:n.-54-868C>A
NM_032538.2:c.-54-868C>A NP_115927.1:n.-54-868C>A
XM_011514947.2:c.-54-868C>A XP_011513249.1:n.-54-868C>A
XM_017011364.1:c.-54-868C>A XP_016866853.1:n.-54-868C>A
XM_017011365.1:c.-54-868C>A XP_016866854.1:n.-54-868C>A
XM_017011366.1:c.-54-868C>A XP_016866855.1:n.-54-868C>A
XM_017011367.1:c.-54-868C>A XP_016866856.1:n.-54-868C>A
NM_032538.3:c.-54-868C>A MANE Select NP_115927.1:n.-54-868C>A