Canonical Allele Identifier: CA726464504
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1474373646
gnomAD v3: 17-16028817-TC-T
gnomAD v4: 17-16028817-TC-T
MyVariant Identifiers: chr17:g.15932132del (hg19) chr17:g.16028818del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16028818del , CM000679.2:g.16028818del GRCh38
NC_000017.10:g.15932132del , CM000679.1:g.15932132del GRCh37
NC_000017.9:g.15872857del NCBI36
NG_029806.1:g.34439del
NG_047111.1:g.192929del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.*1296del MANE Select ENSP00000261647.5:n.*1296del
ENST00000261647.9:c.*1296del ENSP00000261647.5:n.*1296del
ENST00000470649.1:c.247+2116del ENSP00000465627.1:n.247+2116del
NM_001271420.1:c.*1296del NP_001258349.1:n.*1296del
NM_017775.3:c.*1296del NP_060245.3:n.*1296del
XM_017024801.2:c.994+2116del XP_016880290.2:n.994+2116del
XM_017024802.2:c.994+2116del XP_016880291.2:n.994+2116del
NM_017775.4:c.*1296del MANE Select NP_060245.3:n.*1296del
NM_001271420.2:c.*1296del NP_001258349.1:n.*1296del
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