Canonical Allele Identifier: CA2249870801

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028221_16028223delinsCTG , CM000679.2:g.16028221_16028223delinsCTG	GRCh38
NC_000017.10:g.15931535_15931537delinsCTG , CM000679.1:g.15931535_15931537delinsCTG	GRCh37
NC_000017.9:g.15872260_15872262delinsCTG	NCBI36
NG_029806.1:g.33842_33844delinsCTG
NG_047111.1:g.193524_193526delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*699_*701delinsCTG MANE Select	ENSP00000261647.5:n.*699_*701delinsCTG
ENST00000261647.9:c.*699_*701delinsCTG	ENSP00000261647.5:n.*699_*701delinsCTG
ENST00000465567.1:n.2236_2238delinsCTG
ENST00000470649.1:c.247+1519_247+1521delinsCTG	ENSP00000465627.1:n.247+1519_247+1521delinsCTG
ENST00000475723.5:c.2026_2028delinsCTG
ENST00000481107.1:n.2510_2512delinsCTG
NM_001271420.1:c.*699_*701delinsCTG	NP_001258349.1:n.*699_*701delinsCTG
NM_017775.3:c.*699_*701delinsCTG	NP_060245.3:n.*699_*701delinsCTG
XM_017024801.2:c.994+1519_994+1521delinsCTG	XP_016880290.2:n.994+1519_994+1521delinsCTG
XM_017024802.2:c.994+1519_994+1521delinsCTG	XP_016880291.2:n.994+1519_994+1521delinsCTG
NM_017775.4:c.*699_*701delinsCTG MANE Select	NP_060245.3:n.*699_*701delinsCTG
NM_001271420.2:c.*699_*701delinsCTG	NP_001258349.1:n.*699_*701delinsCTG