Canonical Allele Identifier: CA1146489039
Gene: TTC34 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792703T= , CM000663.2:g.2792703T= GRCh38
NC_000001.10:g.2709268T= , CM000663.1:g.2709268T= GRCh37
NC_000001.9:g.2699128T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2357A= MANE Select ENSP00000383873.4:n.785-2357A=
ENST00000401095.8:c.785-2357A= ENSP00000383873.4:n.785-2357A=
NM_001242672.2:c.785-2357A= NP_001229601.2:n.785-2357A=
NM_001242672.3:c.785-2357A= MANE Select NP_001229601.2:n.785-2357A=
Search 100 bp 5'
Search 100 bp 3'