Canonical Allele Identifier: CA708599794

Gene: TTLL5

Linked Data

• dbSNP Id: rs1342677581
• MyVariant Identifiers: chr14:g.76173691_76173692insA (hg19) ; chr14:g.75707348_75707349insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75707349dup , CM000676.2:g.75707349dup	GRCh38
NC_000014.8:g.76173692dup , CM000676.1:g.76173692dup	GRCh37
NC_000014.7:g.75243445dup	NCBI36
NG_016974.1:g.51142dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298832.14:c.655+262dup MANE Select	ENSP00000298832.9:n.655+262dup
ENST00000286650.9:c.655+262dup	ENSP00000286650.5:n.655+262dup
ENST00000298832.13:c.655+262dup	ENSP00000298832.9:n.655+262dup
ENST00000555422.5:n.124+262dup
ENST00000556173.5:n.581+262dup
ENST00000557636.5:c.655+262dup	ENSP00000450713.1:n.655+262dup
NM_015072.4:c.655+262dup	NP_055887.3:n.655+262dup
NM_015072.5:c.655+262dup MANE Select	NP_055887.3:n.655+262dup