Canonical Allele Identifier: CA2249815039

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000021_16000024delinsCGCT , CM000679.2:g.16000021_16000024delinsCGCT	GRCh38
NC_000017.10:g.15903335_15903338delinsCGCT , CM000679.1:g.15903335_15903338delinsCGCT	GRCh37
NC_000017.9:g.15844060_15844063delinsCGCT	NCBI36
NG_029806.1:g.5642_5645delinsCGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.173_176delinsCGCT MANE Select	ENSP00000261647.5:p.Pro58=
ENST00000261647.9:c.173_176delinsCGCT	ENSP00000261647.5:p.Pro58=
ENST00000466729.5:c.238_241delinsCGCT
ENST00000470399.1:c.188_191delinsCGCT	ENSP00000465082.1:p.Pro63=
ENST00000475723.5:c.220_223delinsCGCT
ENST00000497842.6:n.198_201delinsCGCT
ENST00000583704.1:n.198_201delinsCGCT
NM_001271420.1:c.-286_-283delinsCGCT	NP_001258349.1:n.-286_-283delinsCGCT
NM_017775.3:c.173_176delinsCGCT	NP_060245.3:p.Pro58=
XM_011523950.1:c.173_176delinsCGCT	XP_011522252.1:p.Pro58=
XM_017024801.2:c.173_176delinsCGCT	XP_016880290.2:p.Pro58=
XM_017024802.2:c.173_176delinsCGCT	XP_016880291.2:p.Pro58=
XM_024450814.1:c.173_176delinsCGCT	XP_024306582.1:p.Pro58=
NM_017775.4:c.173_176delinsCGCT MANE Select	NP_060245.3:p.Pro58=
NM_001271420.2:c.-286_-283delinsCGCT	NP_001258349.1:n.-286_-283delinsCGCT