Canonical Allele Identifier: CA2742211511
Gene: TTC34 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792672T>C , CM000663.2:g.2792672T>C GRCh38
NC_000001.10:g.2709237T>C , CM000663.1:g.2709237T>C GRCh37
NC_000001.9:g.2699097T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2326A>G MANE Select ENSP00000383873.4:n.785-2326A>G
ENST00000401095.8:c.785-2326A>G ENSP00000383873.4:n.785-2326A>G
NM_001242672.2:c.785-2326A>G NP_001229601.2:n.785-2326A>G
NM_001242672.3:c.785-2326A>G MANE Select NP_001229601.2:n.785-2326A>G