Canonical Allele Identifier: CA981832128

Gene: TTC19

Linked Data

• gnomAD v3: 17-16028766-A-ACGGCGACC
• gnomAD v4: 17-16028766-A-ACGGCGACC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028766_16028767insCGGCGACC , CM000679.2:g.16028766_16028767insCGGCGACC	GRCh38
NC_000017.10:g.15932080_15932081insCGGCGACC , CM000679.1:g.15932080_15932081insCGGCGACC	GRCh37
NC_000017.9:g.15872805_15872806insCGGCGACC	NCBI36
NG_029806.1:g.34387_34388insCGGCGACC
NG_047111.1:g.192980_192981insGGTCGCCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*1244_*1245insCGGCGACC MANE Select	ENSP00000261647.5:n.*1244_*1245insCGGCGACC
ENST00000261647.9:c.*1244_*1245insCGGCGACC	ENSP00000261647.5:n.*1244_*1245insCGGCGACC
ENST00000465567.1:n.2781_2782insCGGCGACC
ENST00000470649.1:c.247+2064_247+2065insCGGCGACC	ENSP00000465627.1:n.247+2064_247+2065insCGGCGACC
ENST00000475723.5:c.2571_2572insCGGCGACC
ENST00000481107.1:n.3055_3056insCGGCGACC
NM_001271420.1:c.*1244_*1245insCGGCGACC	NP_001258349.1:n.*1244_*1245insCGGCGACC
NM_017775.3:c.*1244_*1245insCGGCGACC	NP_060245.3:n.*1244_*1245insCGGCGACC
XM_017024801.2:c.994+2064_994+2065insCGGCGACC	XP_016880290.2:n.994+2064_994+2065insCGGCGACC
XM_017024802.2:c.994+2064_994+2065insCGGCGACC	XP_016880291.2:n.994+2064_994+2065insCGGCGACC
NM_017775.4:c.*1244_*1245insCGGCGACC MANE Select	NP_060245.3:n.*1244_*1245insCGGCGACC
NM_001271420.2:c.*1244_*1245insCGGCGACC	NP_001258349.1:n.*1244_*1245insCGGCGACC