Canonical Allele Identifier: CA2147608670
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs1886740229
gnomAD v4: 14-75707473-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707473C>G , CM000676.2:g.75707473C>G GRCh38
NC_000014.8:g.76173816C>G , CM000676.1:g.76173816C>G GRCh37
NC_000014.7:g.75243569C>G NCBI36
NG_016974.1:g.51266C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000298832.14:c.656-150C>G MANE Select ENSP00000298832.9:n.656-150C>G
ENST00000286650.9:c.656-150C>G ENSP00000286650.5:n.656-150C>G
ENST00000298832.13:c.656-150C>G ENSP00000298832.9:n.656-150C>G
ENST00000555422.5:n.125-150C>G
ENST00000556173.5:n.582-150C>G
ENST00000557636.5:c.656-150C>G ENSP00000450713.1:n.656-150C>G
NM_015072.4:c.656-150C>G NP_055887.3:n.656-150C>G
NM_015072.5:c.656-150C>G MANE Select NP_055887.3:n.656-150C>G
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