Canonical Allele Identifier: CA2249815044

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000035_16000072delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC , CM000679.2:g.16000035_16000072delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	GRCh38
NC_000017.10:g.15903349_15903386delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC , CM000679.1:g.15903349_15903386delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	GRCh37
NC_000017.9:g.15844074_15844111delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	NCBI36
NG_029806.1:g.5656_5693delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC MANE Select	ENSP00000261647.5:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGC...
ENST00000261647.9:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	ENSP00000261647.5:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGC...
ENST00000466729.5:c.249+3_249+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC
ENST00000470399.1:c.199+3_199+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	ENSP00000465082.1:n.199+3_199+40delinsGAGGGGCGCGGGCCGGGCGGGGC...
ENST00000475723.5:c.231+3_231+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC
ENST00000497842.6:n.212_249delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC
ENST00000583704.1:n.209+3_209+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC
NM_001271420.1:c.-275+3_-275+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	NP_001258349.1:n.-275+3_-275+40delinsGAGGGGCGCGGGCCGGGCGGGGCC...
NM_017775.3:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	NP_060245.3:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCG...
XM_011523950.1:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	XP_011522252.1:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGG...
XM_017024801.2:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	XP_016880290.2:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGG...
XM_017024802.2:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	XP_016880291.2:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGG...
XM_024450814.1:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	XP_024306582.1:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGG...
NM_017775.4:c.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC MANE Select	NP_060245.3:n.184+3_184+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCG...
NM_001271420.2:c.-275+3_-275+40delinsGAGGGGCGCGGGCCGGGCGGGGCCGGCCGGGCGGGGAC	NP_001258349.1:n.-275+3_-275+40delinsGAGGGGCGCGGGCCGGGCGGGGCC...