Canonical Allele Identifier: CA498040250

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15930743G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027429G>C , CM000679.2:g.16027429G>C	GRCh38
NC_000017.10:g.15930743G>C , CM000679.1:g.15930743G>C	GRCh37
NC_000017.9:g.15871468G>C	NCBI36
NG_029806.1:g.33050G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1050G>C MANE Select	ENSP00000261647.5:p.Leu350=
ENST00000261647.9:c.1050G>C	ENSP00000261647.5:p.Leu350=
ENST00000465567.1:n.1444G>C
ENST00000470649.1:c.247+727G>C	ENSP00000465627.1:n.247+727G>C
ENST00000475723.5:c.1234G>C
ENST00000481107.1:n.1718G>C
ENST00000497842.6:n.1254G>C
NM_001271420.1:c.729G>C	NP_001258349.1:p.Leu243=
NM_017775.3:c.1050G>C	NP_060245.3:p.Leu350=
XM_017024801.2:c.994+727G>C	XP_016880290.2:n.994+727G>C
XM_017024802.2:c.994+727G>C	XP_016880291.2:n.994+727G>C
NM_017775.4:c.1050G>C MANE Select	NP_060245.3:p.Leu350=
NM_001271420.2:c.729G>C	NP_001258349.1:p.Leu243=