Canonical Allele Identifier: CA2249871774
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16028761A= , CM000679.2:g.16028761A= GRCh38
NC_000017.10:g.15932075A= , CM000679.1:g.15932075A= GRCh37
NC_000017.9:g.15872800A= NCBI36
NG_029806.1:g.34382A=
NG_047111.1:g.192986T=

Transcript Alleles

HGVS Amino-acid change
ENST00000261647.10:c.*1239A= MANE Select ENSP00000261647.5:n.*1239A=
ENST00000261647.9:c.*1239A= ENSP00000261647.5:n.*1239A=
ENST00000465567.1:n.2776A=
ENST00000470649.1:c.247+2059A= ENSP00000465627.1:n.247+2059A=
ENST00000475723.5:c.2566A=
ENST00000481107.1:n.3050A=
NM_001271420.1:c.*1239A= NP_001258349.1:n.*1239A=
NM_017775.3:c.*1239A= NP_060245.3:n.*1239A=
XM_017024801.2:c.994+2059A= XP_016880290.2:n.994+2059A=
XM_017024802.2:c.994+2059A= XP_016880291.2:n.994+2059A=
NM_017775.4:c.*1239A= MANE Select NP_060245.3:n.*1239A=
NM_001271420.2:c.*1239A= NP_001258349.1:n.*1239A=