Canonical Allele Identifier: CA2249869982

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027580_16027582delinsCTG , CM000679.2:g.16027580_16027582delinsCTG	GRCh38
NC_000017.10:g.15930894_15930896delinsCTG , CM000679.1:g.15930894_15930896delinsCTG	GRCh37
NC_000017.9:g.15871619_15871621delinsCTG	NCBI36
NG_029806.1:g.33201_33203delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*58_*60delinsCTG MANE Select	ENSP00000261647.5:n.*58_*60delinsCTG
ENST00000261647.9:c.*58_*60delinsCTG	ENSP00000261647.5:n.*58_*60delinsCTG
ENST00000465567.1:n.1595_1597delinsCTG
ENST00000470649.1:c.247+878_247+880delinsCTG	ENSP00000465627.1:n.247+878_247+880delinsCTG
ENST00000475723.5:c.1385_1387delinsCTG
ENST00000481107.1:n.1869_1871delinsCTG
NM_001271420.1:c.*58_*60delinsCTG	NP_001258349.1:n.*58_*60delinsCTG
NM_017775.3:c.*58_*60delinsCTG	NP_060245.3:n.*58_*60delinsCTG
XM_017024801.2:c.994+878_994+880delinsCTG	XP_016880290.2:n.994+878_994+880delinsCTG
XM_017024802.2:c.994+878_994+880delinsCTG	XP_016880291.2:n.994+878_994+880delinsCTG
NM_017775.4:c.*58_*60delinsCTG MANE Select	NP_060245.3:n.*58_*60delinsCTG
NM_001271420.2:c.*58_*60delinsCTG	NP_001258349.1:n.*58_*60delinsCTG