Canonical Allele Identifier: CA2249871242
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16028521T= , CM000679.2:g.16028521T= GRCh38
NC_000017.10:g.15931835T= , CM000679.1:g.15931835T= GRCh37
NC_000017.9:g.15872560T= NCBI36
NG_029806.1:g.34142T=
NG_047111.1:g.193226A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.*999T= MANE Select ENSP00000261647.5:n.*999T=
ENST00000261647.9:c.*999T= ENSP00000261647.5:n.*999T=
ENST00000465567.1:n.2536T=
ENST00000470649.1:c.247+1819T= ENSP00000465627.1:n.247+1819T=
ENST00000475723.5:c.2326T=
ENST00000481107.1:n.2810T=
NM_001271420.1:c.*999T= NP_001258349.1:n.*999T=
NM_017775.3:c.*999T= NP_060245.3:n.*999T=
XM_017024801.2:c.994+1819T= XP_016880290.2:n.994+1819T=
XM_017024802.2:c.994+1819T= XP_016880291.2:n.994+1819T=
NM_017775.4:c.*999T= MANE Select NP_060245.3:n.*999T=
NM_001271420.2:c.*999T= NP_001258349.1:n.*999T=