Canonical Allele Identifier: CA2249871228

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028510_16028512delinsCTT , CM000679.2:g.16028510_16028512delinsCTT	GRCh38
NC_000017.10:g.15931824_15931826delinsCTT , CM000679.1:g.15931824_15931826delinsCTT	GRCh37
NC_000017.9:g.15872549_15872551delinsCTT	NCBI36
NG_029806.1:g.34131_34133delinsCTT
NG_047111.1:g.193235_193237delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*988_*990delinsCTT MANE Select	ENSP00000261647.5:n.*988_*990delinsCTT
ENST00000261647.9:c.*988_*990delinsCTT	ENSP00000261647.5:n.*988_*990delinsCTT
ENST00000465567.1:n.2525_2527delinsCTT
ENST00000470649.1:c.247+1808_247+1810delinsCTT	ENSP00000465627.1:n.247+1808_247+1810delinsCTT
ENST00000475723.5:c.2315_2317delinsCTT
ENST00000481107.1:n.2799_2801delinsCTT
NM_001271420.1:c.*988_*990delinsCTT	NP_001258349.1:n.*988_*990delinsCTT
NM_017775.3:c.*988_*990delinsCTT	NP_060245.3:n.*988_*990delinsCTT
XM_017024801.2:c.994+1808_994+1810delinsCTT	XP_016880290.2:n.994+1808_994+1810delinsCTT
XM_017024802.2:c.994+1808_994+1810delinsCTT	XP_016880291.2:n.994+1808_994+1810delinsCTT
NM_017775.4:c.*988_*990delinsCTT MANE Select	NP_060245.3:n.*988_*990delinsCTT
NM_001271420.2:c.*988_*990delinsCTT	NP_001258349.1:n.*988_*990delinsCTT