Canonical Allele Identifier: CA2249815025

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000002_16000003delinsCG , CM000679.2:g.16000002_16000003delinsCG	GRCh38
NC_000017.10:g.15903316_15903317delinsCG , CM000679.1:g.15903316_15903317delinsCG	GRCh37
NC_000017.9:g.15844041_15844042delinsCG	NCBI36
NG_029806.1:g.5623_5624delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.154_155delinsCG MANE Select	ENSP00000261647.5:p.Arg52=
ENST00000261647.9:c.154_155delinsCG	ENSP00000261647.5:p.Arg52=
ENST00000466729.5:c.219_220delinsCG
ENST00000470399.1:c.169_170delinsCG	ENSP00000465082.1:p.Arg57=
ENST00000475723.5:c.201_202delinsCG
ENST00000497842.6:n.179_180delinsCG
ENST00000583704.1:n.179_180delinsCG
NM_001271420.1:c.-305_-304delinsCG	NP_001258349.1:n.-305_-304delinsCG
NM_017775.3:c.154_155delinsCG	NP_060245.3:p.Arg52=
XM_011523950.1:c.154_155delinsCG	XP_011522252.1:p.Arg52=
XM_017024801.2:c.154_155delinsCG	XP_016880290.2:p.Arg52=
XM_017024802.2:c.154_155delinsCG	XP_016880291.2:p.Arg52=
XM_024450814.1:c.154_155delinsCG	XP_024306582.1:p.Arg52=
NM_017775.4:c.154_155delinsCG MANE Select	NP_060245.3:p.Arg52=
NM_001271420.2:c.-305_-304delinsCG	NP_001258349.1:n.-305_-304delinsCG