Canonical Allele Identifier: CA615068104

Gene: TTLL5

Linked Data

• dbSNP Id: rs1391120509
• gnomAD v2: 14-76173697-CAT-C
• gnomAD v3: 14-75707354-CAT-C
• gnomAD v4: 14-75707354-CAT-C
• MyVariant Identifiers: chr14:g.76173698_76173699del (hg19) ; chr14:g.75707355_75707356del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.75707357_75707358del , CM000676.2:g.75707357_75707358del	GRCh38
NC_000014.8:g.76173700_76173701del , CM000676.1:g.76173700_76173701del	GRCh37
NC_000014.7:g.75243453_75243454del	NCBI36
NG_016974.1:g.51150_51151del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298832.14:c.656-266_656-265del MANE Select	ENSP00000298832.9:n.656-266_656-265del
ENST00000286650.9:c.656-266_656-265del	ENSP00000286650.5:n.656-266_656-265del
ENST00000298832.13:c.656-266_656-265del	ENSP00000298832.9:n.656-266_656-265del
ENST00000555422.5:n.125-266_125-265del
ENST00000556173.5:n.582-266_582-265del
ENST00000557636.5:c.656-266_656-265del	ENSP00000450713.1:n.656-266_656-265del
NM_015072.4:c.656-266_656-265del	NP_055887.3:n.656-266_656-265del
NM_015072.5:c.656-266_656-265del MANE Select	NP_055887.3:n.656-266_656-265del