Canonical Allele Identifier: CA1121624829
Gene: TTC39B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15282823_15282826del , CM000671.2:g.15282823_15282826del GRCh38
NC_000009.11:g.15282821_15282824del , CM000671.1:g.15282821_15282824del GRCh37
NC_000009.10:g.15272821_15272824del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297615.10:c.43-14878_43-14875del ENSP00000297615.6:n.43-14878_43-14875del
ENST00000380850.9:c.43-14878_43-14875del ENSP00000370231.5:n.43-14878_43-14875del
ENST00000512701.7:c.43-14878_43-14875del MANE Select ENSP00000422496.2:n.43-14878_43-14875del
ENST00000297615.9:c.241-14878_241-14875del ENSP00000297615.5:n.241-14878_241-14875del
ENST00000380850.8:c.241-14878_241-14875del ENSP00000370231.4:n.241-14878_241-14875del
ENST00000505732.5:n.278-14878_278-14875del
ENST00000506891.1:c.127-14878_127-14875del ENSP00000427314.1:n.127-14878_127-14875del
ENST00000512701.6:c.241-14878_241-14875del ENSP00000422496.1:n.241-14878_241-14875del
NM_001168339.1:c.241-14878_241-14875del NP_001161811.1:n.241-14878_241-14875del
NM_001168340.1:c.241-14878_241-14875del NP_001161812.1:n.241-14878_241-14875del
NM_001168341.1:c.241-14878_241-14875del NP_001161813.1:n.241-14878_241-14875del
NM_152574.2:c.241-14878_241-14875del NP_689787.2:n.241-14878_241-14875del
XM_011517733.1:c.241-14878_241-14875del XP_011516035.1:n.241-14878_241-14875del
XM_017014310.1:c.-112-14363_-112-14360del XP_016869799.1:n.-112-14363_-112-14360del
XM_017014311.1:c.-221-14363_-221-14360del XP_016869800.1:n.-221-14363_-221-14360del
XM_024447422.1:c.-51-14878_-51-14875del XP_024303190.1:n.-51-14878_-51-14875del
XR_001746190.1:n.278-14878_278-14875del
NM_001168339.2:c.43-14878_43-14875del NP_001161811.2:n.43-14878_43-14875del
NM_001168340.2:c.43-14878_43-14875del NP_001161812.2:n.43-14878_43-14875del
NM_001168341.2:c.43-14878_43-14875del NP_001161813.2:n.43-14878_43-14875del
NM_152574.3:c.43-14878_43-14875del MANE Select NP_689787.3:n.43-14878_43-14875del