Canonical Allele Identifier: CA708599806

Gene: TTLL5

Linked Data

• dbSNP Id: rs1370028763
• gnomAD v3: 14-75707398-CATT-C
• gnomAD v4: 14-75707398-CATT-C
• MyVariant Identifiers: chr14:g.76173742_76173744del (hg19) ; chr14:g.75707399_75707401del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75707401_75707403del , CM000676.2:g.75707401_75707403del	GRCh38
NC_000014.8:g.76173744_76173746del , CM000676.1:g.76173744_76173746del	GRCh37
NC_000014.7:g.75243497_75243499del	NCBI36
NG_016974.1:g.51194_51196del

Transcript Alleles

HGVS	Amino-acid change
ENST00000298832.14:c.656-222_656-220del MANE Select	ENSP00000298832.9:n.656-222_656-220del
ENST00000286650.9:c.656-222_656-220del	ENSP00000286650.5:n.656-222_656-220del
ENST00000298832.13:c.656-222_656-220del	ENSP00000298832.9:n.656-222_656-220del
ENST00000555422.5:n.125-222_125-220del
ENST00000556173.5:n.582-222_582-220del
ENST00000557636.5:c.656-222_656-220del	ENSP00000450713.1:n.656-222_656-220del
NM_015072.4:c.656-222_656-220del	NP_055887.3:n.656-222_656-220del
NM_015072.5:c.656-222_656-220del MANE Select	NP_055887.3:n.656-222_656-220del