Canonical Allele Identifier: CA398379434
Gene: TTC19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16027492T>G , CM000679.2:g.16027492T>G GRCh38
NC_000017.10:g.15930806T>G , CM000679.1:g.15930806T>G GRCh37
NC_000017.9:g.15871531T>G NCBI36
NG_029806.1:g.33113T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.1113T>G MANE Select ENSP00000261647.5:p.Ser371Arg
ENST00000261647.9:c.1113T>G ENSP00000261647.5:p.Ser371Arg
ENST00000465567.1:n.1507T>G
ENST00000470649.1:c.247+790T>G ENSP00000465627.1:n.247+790T>G
ENST00000475723.5:c.1297T>G
ENST00000481107.1:n.1781T>G
ENST00000497842.6:n.1317T>G
NM_001271420.1:c.792T>G NP_001258349.1:p.Ser264Arg
NM_017775.3:c.1113T>G NP_060245.3:p.Ser371Arg
XM_017024801.2:c.994+790T>G XP_016880290.2:n.994+790T>G
XM_017024802.2:c.994+790T>G XP_016880291.2:n.994+790T>G
NM_017775.4:c.1113T>G MANE Select NP_060245.3:p.Ser371Arg
NM_001271420.2:c.792T>G NP_001258349.1:p.Ser264Arg