Canonical Allele Identifier: CA1149825998
Gene: TTC34 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.2792671G= , CM000663.2:g.2792671G= GRCh38
NC_000001.10:g.2709236G= , CM000663.1:g.2709236G= GRCh37
NC_000001.9:g.2699096G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000401095.9:c.785-2325C= MANE Select ENSP00000383873.4:n.785-2325C=
ENST00000401095.8:c.785-2325C= ENSP00000383873.4:n.785-2325C=
NM_001242672.2:c.785-2325C= NP_001229601.2:n.785-2325C=
NM_001242672.3:c.785-2325C= MANE Select NP_001229601.2:n.785-2325C=
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