Canonical Allele Identifier: CA288164807

Gene: TTC19

Linked Data

• dbSNP Id: rs766912323
• MyVariant Identifiers: chr17:g.15930901_15930902del (hg19) ; chr17:g.16027587_16027588del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027589_16027590del , CM000679.2:g.16027589_16027590del	GRCh38
NC_000017.10:g.15930903_15930904del , CM000679.1:g.15930903_15930904del	GRCh37
NC_000017.9:g.15871628_15871629del	NCBI36
NG_029806.1:g.33210_33211del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*67_*68del MANE Select	ENSP00000261647.5:n.*67_*68del
ENST00000261647.9:c.*67_*68del	ENSP00000261647.5:n.*67_*68del
ENST00000465567.1:n.1604_1605del
ENST00000470649.1:c.247+887_247+888del	ENSP00000465627.1:n.247+887_247+888del
ENST00000475723.5:c.1394_1395del
ENST00000481107.1:n.1878_1879del
NM_001271420.1:c.*67_*68del	NP_001258349.1:n.*67_*68del
NM_017775.3:c.*67_*68del	NP_060245.3:n.*67_*68del
XM_017024801.2:c.994+887_994+888del	XP_016880290.2:n.994+887_994+888del
XM_017024802.2:c.994+887_994+888del	XP_016880291.2:n.994+887_994+888del
NM_017775.4:c.*67_*68del MANE Select	NP_060245.3:n.*67_*68del
NM_001271420.2:c.*67_*68del	NP_001258349.1:n.*67_*68del