Canonical Allele Identifier: CA2636262418

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027645-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027645T>A , CM000679.2:g.16027645T>A	GRCh38
NC_000017.10:g.15930959T>A , CM000679.1:g.15930959T>A	GRCh37
NC_000017.9:g.15871684T>A	NCBI36
NG_029806.1:g.33266T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*123T>A MANE Select	ENSP00000261647.5:n.*123T>A
ENST00000261647.9:c.*123T>A	ENSP00000261647.5:n.*123T>A
ENST00000465567.1:n.1660T>A
ENST00000470649.1:c.247+943T>A	ENSP00000465627.1:n.247+943T>A
ENST00000475723.5:c.1450T>A
ENST00000481107.1:n.1934T>A
NM_001271420.1:c.*123T>A	NP_001258349.1:n.*123T>A
NM_017775.3:c.*123T>A	NP_060245.3:n.*123T>A
XM_017024801.2:c.994+943T>A	XP_016880290.2:n.994+943T>A
XM_017024802.2:c.994+943T>A	XP_016880291.2:n.994+943T>A
NM_017775.4:c.*123T>A MANE Select	NP_060245.3:n.*123T>A
NM_001271420.2:c.*123T>A	NP_001258349.1:n.*123T>A