Canonical Allele Identifier: CA2636262918

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028494-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028495dup , CM000679.2:g.16028495dup	GRCh38
NC_000017.10:g.15931809dup , CM000679.1:g.15931809dup	GRCh37
NC_000017.9:g.15872534dup	NCBI36
NG_029806.1:g.34116dup
NG_047111.1:g.193252dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*973dup MANE Select	ENSP00000261647.5:n.*973dup
ENST00000261647.9:c.*973dup	ENSP00000261647.5:n.*973dup
ENST00000465567.1:n.2510dup
ENST00000470649.1:c.247+1793dup	ENSP00000465627.1:n.247+1793dup
ENST00000475723.5:c.2300dup
ENST00000481107.1:n.2784dup
NM_001271420.1:c.*973dup	NP_001258349.1:n.*973dup
NM_017775.3:c.*973dup	NP_060245.3:n.*973dup
XM_017024801.2:c.994+1793dup	XP_016880290.2:n.994+1793dup
XM_017024802.2:c.994+1793dup	XP_016880291.2:n.994+1793dup
NM_017775.4:c.*973dup MANE Select	NP_060245.3:n.*973dup
NM_001271420.2:c.*973dup	NP_001258349.1:n.*973dup