Canonical Allele Identifier: CA288164801

Gene: TTC19

Linked Data

• dbSNP Id: rs1036823411
• gnomAD v3: 17-16027581-T-A
• gnomAD v4: 17-16027581-T-A
• MyVariant Identifiers: chr17:g.15930895T>A (hg19) ; chr17:g.16027581T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027581T>A , CM000679.2:g.16027581T>A	GRCh38
NC_000017.10:g.15930895T>A , CM000679.1:g.15930895T>A	GRCh37
NC_000017.9:g.15871620T>A	NCBI36
NG_029806.1:g.33202T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*59T>A MANE Select	ENSP00000261647.5:n.*59T>A
ENST00000261647.9:c.*59T>A	ENSP00000261647.5:n.*59T>A
ENST00000465567.1:n.1596T>A
ENST00000470649.1:c.247+879T>A	ENSP00000465627.1:n.247+879T>A
ENST00000475723.5:c.1386T>A
ENST00000481107.1:n.1870T>A
NM_001271420.1:c.*59T>A	NP_001258349.1:n.*59T>A
NM_017775.3:c.*59T>A	NP_060245.3:n.*59T>A
XM_017024801.2:c.994+879T>A	XP_016880290.2:n.994+879T>A
XM_017024802.2:c.994+879T>A	XP_016880291.2:n.994+879T>A
NM_017775.4:c.*59T>A MANE Select	NP_060245.3:n.*59T>A
NM_001271420.2:c.*59T>A	NP_001258349.1:n.*59T>A