Canonical Allele Identifier: CA615068108
Gene: TTLL5 HGNC NCBI

Linked Data

dbSNP Id: rs1341116495
gnomAD v2: 14-76173817-C-T
gnomAD v3: 14-75707474-C-T
gnomAD v4: 14-75707474-C-T
MyVariant Identifiers: chr14:g.76173817C>T (hg19) chr14:g.75707474C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.75707474C>T , CM000676.2:g.75707474C>T GRCh38
NC_000014.8:g.76173817C>T , CM000676.1:g.76173817C>T GRCh37
NC_000014.7:g.75243570C>T NCBI36
NG_016974.1:g.51267C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000298832.14:c.656-149C>T MANE Select ENSP00000298832.9:n.656-149C>T
ENST00000286650.9:c.656-149C>T ENSP00000286650.5:n.656-149C>T
ENST00000298832.13:c.656-149C>T ENSP00000298832.9:n.656-149C>T
ENST00000555422.5:n.125-149C>T
ENST00000556173.5:n.582-149C>T
ENST00000557636.5:c.656-149C>T ENSP00000450713.1:n.656-149C>T
NM_015072.4:c.656-149C>T NP_055887.3:n.656-149C>T
NM_015072.5:c.656-149C>T MANE Select NP_055887.3:n.656-149C>T
Search 100 bp 5'
Search 100 bp 3'