Canonical Allele Identifier: CA398382293
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1489735442

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999933C>T , CM000679.2:g.15999933C>T GRCh38
NC_000017.10:g.15903247C>T , CM000679.1:g.15903247C>T GRCh37
NC_000017.9:g.15843972C>T NCBI36
NG_029806.1:g.5554C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.85C>T MANE Select ENSP00000261647.5:p.Leu29Phe
ENST00000261647.9:c.85C>T ENSP00000261647.5:p.Leu29Phe
ENST00000466729.5:c.150C>T
ENST00000470399.1:c.100C>T ENSP00000465082.1:p.Leu34Phe
ENST00000475723.5:c.132C>T
ENST00000497842.6:n.110C>T
ENST00000583704.1:n.110C>T
NM_001271420.1:c.-374C>T NP_001258349.1:n.-374C>T
NM_017775.3:c.85C>T NP_060245.3:p.Leu29Phe
XM_011523950.1:c.85C>T XP_011522252.1:p.Leu29Phe
XM_017024801.2:c.85C>T XP_016880290.2:p.Leu29Phe
XM_017024802.2:c.85C>T XP_016880291.2:p.Leu29Phe
XM_024450814.1:c.85C>T XP_024306582.1:p.Leu29Phe
NM_017775.4:c.85C>T MANE Select NP_060245.3:p.Leu29Phe
NM_001271420.2:c.-374C>T NP_001258349.1:n.-374C>T