Canonical Allele Identifier: CA981832178
Gene: TTC19 HGNC NCBI

Linked Data

gnomAD v3: 17-16028815-T-G
gnomAD v4: 17-16028815-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16028815T>G , CM000679.2:g.16028815T>G GRCh38
NC_000017.10:g.15932129T>G , CM000679.1:g.15932129T>G GRCh37
NC_000017.9:g.15872854T>G NCBI36
NG_029806.1:g.34436T>G
NG_047111.1:g.192932A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.*1293T>G MANE Select ENSP00000261647.5:n.*1293T>G
ENST00000261647.9:c.*1293T>G ENSP00000261647.5:n.*1293T>G
ENST00000470649.1:c.247+2113T>G ENSP00000465627.1:n.247+2113T>G
NM_001271420.1:c.*1293T>G NP_001258349.1:n.*1293T>G
NM_017775.3:c.*1293T>G NP_060245.3:n.*1293T>G
XM_017024801.2:c.994+2113T>G XP_016880290.2:n.994+2113T>G
XM_017024802.2:c.994+2113T>G XP_016880291.2:n.994+2113T>G
NM_017775.4:c.*1293T>G MANE Select NP_060245.3:n.*1293T>G
NM_001271420.2:c.*1293T>G NP_001258349.1:n.*1293T>G
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