Canonical Allele Identifier: CA964833892
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs1886730654
gnomAD v3: 14-75707377-A-G
gnomAD v4: 14-75707377-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707377A>G , CM000676.2:g.75707377A>G GRCh38
NC_000014.8:g.76173720A>G , CM000676.1:g.76173720A>G GRCh37
NC_000014.7:g.75243473A>G NCBI36
NG_016974.1:g.51170A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.656-246A>G MANE Select ENSP00000298832.9:n.656-246A>G
ENST00000286650.9:c.656-246A>G ENSP00000286650.5:n.656-246A>G
ENST00000298832.13:c.656-246A>G ENSP00000298832.9:n.656-246A>G
ENST00000555422.5:n.125-246A>G
ENST00000556173.5:n.582-246A>G
ENST00000557636.5:c.656-246A>G ENSP00000450713.1:n.656-246A>G
NM_015072.4:c.656-246A>G NP_055887.3:n.656-246A>G
NM_015072.5:c.656-246A>G MANE Select NP_055887.3:n.656-246A>G
Search 100 bp 5'
Search 100 bp 3'