Canonical Allele Identifier: CA498414296

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999881-A-G
• MyVariant Identifiers: chr17:g.15903195A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999881A>G , CM000679.2:g.15999881A>G	GRCh38
NC_000017.10:g.15903195A>G , CM000679.1:g.15903195A>G	GRCh37
NC_000017.9:g.15843920A>G	NCBI36
NG_029806.1:g.5502A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.33A>G MANE Select	ENSP00000261647.5:p.Arg11=
ENST00000261647.9:c.33A>G	ENSP00000261647.5:p.Arg11=
ENST00000466729.5:c.98A>G
ENST00000470399.1:c.48A>G	ENSP00000465082.1:p.Arg16=
ENST00000475723.5:c.80A>G
ENST00000497842.6:n.58A>G
ENST00000583704.1:n.58A>G
NM_001271420.1:c.-426A>G	NP_001258349.1:n.-426A>G
NM_017775.3:c.33A>G	NP_060245.3:p.Arg11=
XM_011523950.1:c.33A>G	XP_011522252.1:p.Arg11=
XM_017024801.2:c.33A>G	XP_016880290.2:p.Arg11=
XM_017024802.2:c.33A>G	XP_016880291.2:p.Arg11=
XM_024450814.1:c.33A>G	XP_024306582.1:p.Arg11=
NM_017775.4:c.33A>G MANE Select	NP_060245.3:p.Arg11=
NM_001271420.2:c.-426A>G	NP_001258349.1:n.-426A>G