Canonical Allele Identifier: CA263682907
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs753586153
gnomAD v3: 14-75707548-G-A
gnomAD v4: 14-75707548-G-A
MyVariant Identifiers: chr14:g.76173891G>A (hg19) chr14:g.75707548G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707548G>A , CM000676.2:g.75707548G>A GRCh38
NC_000014.8:g.76173891G>A , CM000676.1:g.76173891G>A GRCh37
NC_000014.7:g.75243644G>A NCBI36
NG_016974.1:g.51341G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000298832.14:c.656-75G>A MANE Select ENSP00000298832.9:n.656-75G>A
ENST00000286650.9:c.656-75G>A ENSP00000286650.5:n.656-75G>A
ENST00000298832.13:c.656-75G>A ENSP00000298832.9:n.656-75G>A
ENST00000555422.5:n.125-75G>A
ENST00000556173.5:n.582-75G>A
ENST00000557636.5:c.656-75G>A ENSP00000450713.1:n.656-75G>A
NM_015072.4:c.656-75G>A NP_055887.3:n.656-75G>A
NM_015072.5:c.656-75G>A MANE Select NP_055887.3:n.656-75G>A
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