Canonical Allele Identifier: CA2147608667

Gene: TTLL5

Linked Data

• dbSNP Id: rs1886739773

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75707467_75707469del , CM000676.2:g.75707467_75707469del	GRCh38
NC_000014.8:g.76173810_76173812del , CM000676.1:g.76173810_76173812del	GRCh37
NC_000014.7:g.75243563_75243565del	NCBI36
NG_016974.1:g.51260_51262del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298832.14:c.656-156_656-154del MANE Select	ENSP00000298832.9:n.656-156_656-154del
ENST00000286650.9:c.656-156_656-154del	ENSP00000286650.5:n.656-156_656-154del
ENST00000298832.13:c.656-156_656-154del	ENSP00000298832.9:n.656-156_656-154del
ENST00000555422.5:n.125-156_125-154del
ENST00000556173.5:n.582-156_582-154del
ENST00000557636.5:c.656-156_656-154del	ENSP00000450713.1:n.656-156_656-154del
NM_015072.4:c.656-156_656-154del	NP_055887.3:n.656-156_656-154del
NM_015072.5:c.656-156_656-154del MANE Select	NP_055887.3:n.656-156_656-154del