Canonical Allele Identifier: CA2249871235
Gene: TTC19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16028514G= , CM000679.2:g.16028514G= GRCh38
NC_000017.10:g.15931828G= , CM000679.1:g.15931828G= GRCh37
NC_000017.9:g.15872553G= NCBI36
NG_029806.1:g.34135G=
NG_047111.1:g.193233C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.*992G= MANE Select ENSP00000261647.5:n.*992G=
ENST00000261647.9:c.*992G= ENSP00000261647.5:n.*992G=
ENST00000465567.1:n.2529G=
ENST00000470649.1:c.247+1812G= ENSP00000465627.1:n.247+1812G=
ENST00000475723.5:c.2319G=
ENST00000481107.1:n.2803G=
NM_001271420.1:c.*992G= NP_001258349.1:n.*992G=
NM_017775.3:c.*992G= NP_060245.3:n.*992G=
XM_017024801.2:c.994+1812G= XP_016880290.2:n.994+1812G=
XM_017024802.2:c.994+1812G= XP_016880291.2:n.994+1812G=
NM_017775.4:c.*992G= MANE Select NP_060245.3:n.*992G=
NM_001271420.2:c.*992G= NP_001258349.1:n.*992G=