Canonical Allele Identifier: CA498040291

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15930818A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027504A>G , CM000679.2:g.16027504A>G	GRCh38
NC_000017.10:g.15930818A>G , CM000679.1:g.15930818A>G	GRCh37
NC_000017.9:g.15871543A>G	NCBI36
NG_029806.1:g.33125A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1125A>G MANE Select	ENSP00000261647.5:p.Thr375=
ENST00000261647.9:c.1125A>G	ENSP00000261647.5:p.Thr375=
ENST00000465567.1:n.1519A>G
ENST00000470649.1:c.247+802A>G	ENSP00000465627.1:n.247+802A>G
ENST00000475723.5:c.1309A>G
ENST00000481107.1:n.1793A>G
ENST00000497842.6:n.1329A>G
NM_001271420.1:c.804A>G	NP_001258349.1:p.Thr268=
NM_017775.3:c.1125A>G	NP_060245.3:p.Thr375=
XM_017024801.2:c.994+802A>G	XP_016880290.2:n.994+802A>G
XM_017024802.2:c.994+802A>G	XP_016880291.2:n.994+802A>G
NM_017775.4:c.1125A>G MANE Select	NP_060245.3:p.Thr375=
NM_001271420.2:c.804A>G	NP_001258349.1:p.Thr268=