Canonical Allele Identifier: CA726464170

Gene: TTC19

Linked Data

• dbSNP Id: rs1338543051
• gnomAD v3: 17-16028459-G-GA
• gnomAD v4: 17-16028459-G-GA
• MyVariant Identifiers: chr17:g.15931773_15931774insA (hg19) ; chr17:g.16028459_16028460insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028462dup , CM000679.2:g.16028462dup	GRCh38
NC_000017.10:g.15931776dup , CM000679.1:g.15931776dup	GRCh37
NC_000017.9:g.15872501dup	NCBI36
NG_029806.1:g.34083dup
NG_047111.1:g.193287dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*940dup MANE Select	ENSP00000261647.5:n.*940dup
ENST00000261647.9:c.*940dup	ENSP00000261647.5:n.*940dup
ENST00000465567.1:n.2477dup
ENST00000470649.1:c.247+1760dup	ENSP00000465627.1:n.247+1760dup
ENST00000475723.5:c.2267dup
ENST00000481107.1:n.2751dup
NM_001271420.1:c.*940dup	NP_001258349.1:n.*940dup
NM_017775.3:c.*940dup	NP_060245.3:n.*940dup
XM_017024801.2:c.994+1760dup	XP_016880290.2:n.994+1760dup
XM_017024802.2:c.994+1760dup	XP_016880291.2:n.994+1760dup
NM_017775.4:c.*940dup MANE Select	NP_060245.3:n.*940dup
NM_001271420.2:c.*940dup	NP_001258349.1:n.*940dup