Canonical Allele Identifier: CA708599857

Gene: TTLL5

Linked Data

• dbSNP Id: rs1162453134
• gnomAD v3: 14-75707469-T-C
• gnomAD v4: 14-75707469-T-C
• MyVariant Identifiers: chr14:g.76173812T>C (hg19) ; chr14:g.75707469T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75707469T>C , CM000676.2:g.75707469T>C	GRCh38
NC_000014.8:g.76173812T>C , CM000676.1:g.76173812T>C	GRCh37
NC_000014.7:g.75243565T>C	NCBI36
NG_016974.1:g.51262T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000298832.14:c.656-154T>C MANE Select	ENSP00000298832.9:n.656-154T>C
ENST00000286650.9:c.656-154T>C	ENSP00000286650.5:n.656-154T>C
ENST00000298832.13:c.656-154T>C	ENSP00000298832.9:n.656-154T>C
ENST00000555422.5:n.125-154T>C
ENST00000556173.5:n.582-154T>C
ENST00000557636.5:c.656-154T>C	ENSP00000450713.1:n.656-154T>C
NM_015072.4:c.656-154T>C	NP_055887.3:n.656-154T>C
NM_015072.5:c.656-154T>C MANE Select	NP_055887.3:n.656-154T>C