Canonical Allele Identifier: CA2249815059

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000046_16000047delinsGC , CM000679.2:g.16000046_16000047delinsGC	GRCh38
NC_000017.10:g.15903360_15903361delinsGC , CM000679.1:g.15903360_15903361delinsGC	GRCh37
NC_000017.9:g.15844085_15844086delinsGC	NCBI36
NG_029806.1:g.5667_5668delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.184+14_184+15delinsGC MANE Select	ENSP00000261647.5:n.184+14_184+15delinsGC
ENST00000261647.9:c.184+14_184+15delinsGC	ENSP00000261647.5:n.184+14_184+15delinsGC
ENST00000466729.5:c.249+14_249+15delinsGC
ENST00000470399.1:c.199+14_199+15delinsGC	ENSP00000465082.1:n.199+14_199+15delinsGC
ENST00000475723.5:c.231+14_231+15delinsGC
ENST00000497842.6:n.223_224delinsGC
ENST00000583704.1:n.209+14_209+15delinsGC
NM_001271420.1:c.-275+14_-275+15delinsGC	NP_001258349.1:n.-275+14_-275+15delinsGC
NM_017775.3:c.184+14_184+15delinsGC	NP_060245.3:n.184+14_184+15delinsGC
XM_011523950.1:c.184+14_184+15delinsGC	XP_011522252.1:n.184+14_184+15delinsGC
XM_017024801.2:c.184+14_184+15delinsGC	XP_016880290.2:n.184+14_184+15delinsGC
XM_017024802.2:c.184+14_184+15delinsGC	XP_016880291.2:n.184+14_184+15delinsGC
XM_024450814.1:c.184+14_184+15delinsGC	XP_024306582.1:n.184+14_184+15delinsGC
NM_017775.4:c.184+14_184+15delinsGC MANE Select	NP_060245.3:n.184+14_184+15delinsGC
NM_001271420.2:c.-275+14_-275+15delinsGC	NP_001258349.1:n.-275+14_-275+15delinsGC