Canonical Allele Identifier: CA726463380

Gene: TTC19

Linked Data

• dbSNP Id: rs1439147338
• MyVariant Identifiers: chr17:g.15930944del (hg19) ; chr17:g.16027630del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027630del , CM000679.2:g.16027630del	GRCh38
NC_000017.10:g.15930944del , CM000679.1:g.15930944del	GRCh37
NC_000017.9:g.15871669del	NCBI36
NG_029806.1:g.33251del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*108del MANE Select	ENSP00000261647.5:n.*108del
ENST00000261647.9:c.*108del	ENSP00000261647.5:n.*108del
ENST00000465567.1:n.1645del
ENST00000470649.1:c.247+928del	ENSP00000465627.1:n.247+928del
ENST00000475723.5:c.1435del
ENST00000481107.1:n.1919del
NM_001271420.1:c.*108del	NP_001258349.1:n.*108del
NM_017775.3:c.*108del	NP_060245.3:n.*108del
XM_017024801.2:c.994+928del	XP_016880290.2:n.994+928del
XM_017024802.2:c.994+928del	XP_016880291.2:n.994+928del
NM_017775.4:c.*108del MANE Select	NP_060245.3:n.*108del
NM_001271420.2:c.*108del	NP_001258349.1:n.*108del