Canonical Allele Identifier: CA2249871232
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16028513T= , CM000679.2:g.16028513T= GRCh38
NC_000017.10:g.15931827T= , CM000679.1:g.15931827T= GRCh37
NC_000017.9:g.15872552T= NCBI36
NG_029806.1:g.34134T=
NG_047111.1:g.193234A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.*991T= MANE Select ENSP00000261647.5:n.*991T=
ENST00000261647.9:c.*991T= ENSP00000261647.5:n.*991T=
ENST00000465567.1:n.2528T=
ENST00000470649.1:c.247+1811T= ENSP00000465627.1:n.247+1811T=
ENST00000475723.5:c.2318T=
ENST00000481107.1:n.2802T=
NM_001271420.1:c.*991T= NP_001258349.1:n.*991T=
NM_017775.3:c.*991T= NP_060245.3:n.*991T=
XM_017024801.2:c.994+1811T= XP_016880290.2:n.994+1811T=
XM_017024802.2:c.994+1811T= XP_016880291.2:n.994+1811T=
NM_017775.4:c.*991T= MANE Select NP_060245.3:n.*991T=
NM_001271420.2:c.*991T= NP_001258349.1:n.*991T=