Canonical Allele Identifier: CA2249815030

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000006_16000007delinsGC , CM000679.2:g.16000006_16000007delinsGC	GRCh38
NC_000017.10:g.15903320_15903321delinsGC , CM000679.1:g.15903320_15903321delinsGC	GRCh37
NC_000017.9:g.15844045_15844046delinsGC	NCBI36
NG_029806.1:g.5627_5628delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.158_159delinsGC MANE Select	ENSP00000261647.5:p.Gly53=
ENST00000261647.9:c.158_159delinsGC	ENSP00000261647.5:p.Gly53=
ENST00000466729.5:c.223_224delinsGC
ENST00000470399.1:c.173_174delinsGC	ENSP00000465082.1:p.Gly58=
ENST00000475723.5:c.205_206delinsGC
ENST00000497842.6:n.183_184delinsGC
ENST00000583704.1:n.183_184delinsGC
NM_001271420.1:c.-301_-300delinsGC	NP_001258349.1:n.-301_-300delinsGC
NM_017775.3:c.158_159delinsGC	NP_060245.3:p.Gly53=
XM_011523950.1:c.158_159delinsGC	XP_011522252.1:p.Gly53=
XM_017024801.2:c.158_159delinsGC	XP_016880290.2:p.Gly53=
XM_017024802.2:c.158_159delinsGC	XP_016880291.2:p.Gly53=
XM_024450814.1:c.158_159delinsGC	XP_024306582.1:p.Gly53=
NM_017775.4:c.158_159delinsGC MANE Select	NP_060245.3:p.Gly53=
NM_001271420.2:c.-301_-300delinsGC	NP_001258349.1:n.-301_-300delinsGC