Canonical Allele Identifier: CA2580583401
Gene: TTC34 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792599C>T , CM000663.2:g.2792599C>T GRCh38
NC_000001.10:g.2709164C>T , CM000663.1:g.2709164C>T GRCh37
NC_000001.9:g.2699024C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2253G>A MANE Select ENSP00000383873.4:n.785-2253G>A
ENST00000401095.8:c.785-2253G>A ENSP00000383873.4:n.785-2253G>A
NM_001242672.2:c.785-2253G>A NP_001229601.2:n.785-2253G>A
NM_001242672.3:c.785-2253G>A MANE Select NP_001229601.2:n.785-2253G>A
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