Canonical Allele Identifier: CA2636262383

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027525-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027525C>A , CM000679.2:g.16027525C>A	GRCh38
NC_000017.10:g.15930839C>A , CM000679.1:g.15930839C>A	GRCh37
NC_000017.9:g.15871564C>A	NCBI36
NG_029806.1:g.33146C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*3C>A MANE Select	ENSP00000261647.5:n.*3C>A
ENST00000261647.9:c.*3C>A	ENSP00000261647.5:n.*3C>A
ENST00000465567.1:n.1540C>A
ENST00000470649.1:c.247+823C>A	ENSP00000465627.1:n.247+823C>A
ENST00000475723.5:c.1330C>A
ENST00000481107.1:n.1814C>A
ENST00000497842.6:n.1350C>A
NM_001271420.1:c.*3C>A	NP_001258349.1:n.*3C>A
NM_017775.3:c.*3C>A	NP_060245.3:n.*3C>A
XM_017024801.2:c.994+823C>A	XP_016880290.2:n.994+823C>A
XM_017024802.2:c.994+823C>A	XP_016880291.2:n.994+823C>A
NM_017775.4:c.*3C>A MANE Select	NP_060245.3:n.*3C>A
NM_001271420.2:c.*3C>A	NP_001258349.1:n.*3C>A