Canonical Allele Identifier: CA498414342

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999929-C-A
• MyVariant Identifiers: chr17:g.15903243C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999929C>A , CM000679.2:g.15999929C>A	GRCh38
NC_000017.10:g.15903243C>A , CM000679.1:g.15903243C>A	GRCh37
NC_000017.9:g.15843968C>A	NCBI36
NG_029806.1:g.5550C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.81C>A MANE Select	ENSP00000261647.5:p.Arg27=
ENST00000261647.9:c.81C>A	ENSP00000261647.5:p.Arg27=
ENST00000466729.5:c.146C>A
ENST00000470399.1:c.96C>A	ENSP00000465082.1:p.Arg32=
ENST00000475723.5:c.128C>A
ENST00000497842.6:n.106C>A
ENST00000583704.1:n.106C>A
NM_001271420.1:c.-378C>A	NP_001258349.1:n.-378C>A
NM_017775.3:c.81C>A	NP_060245.3:p.Arg27=
XM_011523950.1:c.81C>A	XP_011522252.1:p.Arg27=
XM_017024801.2:c.81C>A	XP_016880290.2:p.Arg27=
XM_017024802.2:c.81C>A	XP_016880291.2:p.Arg27=
XM_024450814.1:c.81C>A	XP_024306582.1:p.Arg27=
NM_017775.4:c.81C>A MANE Select	NP_060245.3:p.Arg27=
NM_001271420.2:c.-378C>A	NP_001258349.1:n.-378C>A