Canonical Allele Identifier: CA263682813

Gene: TTLL5

Linked Data

• dbSNP Id: rs906128687
• MyVariant Identifiers: chr14:g.76173742A>G (hg19) ; chr14:g.75707399A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75707399A>G , CM000676.2:g.75707399A>G	GRCh38
NC_000014.8:g.76173742A>G , CM000676.1:g.76173742A>G	GRCh37
NC_000014.7:g.75243495A>G	NCBI36
NG_016974.1:g.51192A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298832.14:c.656-224A>G MANE Select	ENSP00000298832.9:n.656-224A>G
ENST00000286650.9:c.656-224A>G	ENSP00000286650.5:n.656-224A>G
ENST00000298832.13:c.656-224A>G	ENSP00000298832.9:n.656-224A>G
ENST00000555422.5:n.125-224A>G
ENST00000556173.5:n.582-224A>G
ENST00000557636.5:c.656-224A>G	ENSP00000450713.1:n.656-224A>G
NM_015072.4:c.656-224A>G	NP_055887.3:n.656-224A>G
NM_015072.5:c.656-224A>G MANE Select	NP_055887.3:n.656-224A>G