Canonical Allele Identifier: CA726464417

Gene: TTC19

Linked Data

• dbSNP Id: rs1555530985
• gnomAD v3: 17-16028755-A-ATG
• gnomAD v4: 17-16028755-A-ATG
• MyVariant Identifiers: chr17:g.15932069_15932070insTG (hg19) ; chr17:g.16028755_16028756insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028756_16028757insGT , CM000679.2:g.16028756_16028757insGT	GRCh38
NC_000017.10:g.15932070_15932071insGT , CM000679.1:g.15932070_15932071insGT	GRCh37
NC_000017.9:g.15872795_15872796insGT	NCBI36
NG_029806.1:g.34377_34378insGT
NG_047111.1:g.192991_192992insCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*1234_*1235insGT MANE Select	ENSP00000261647.5:n.*1234_*1235insGT
ENST00000261647.9:c.*1234_*1235insGT	ENSP00000261647.5:n.*1234_*1235insGT
ENST00000465567.1:n.2771_2772insGT
ENST00000470649.1:c.247+2054_247+2055insGT	ENSP00000465627.1:n.247+2054_247+2055insGT
ENST00000475723.5:c.2561_2562insGT
ENST00000481107.1:n.3045_3046insGT
NM_001271420.1:c.*1234_*1235insGT	NP_001258349.1:n.*1234_*1235insGT
NM_017775.3:c.*1234_*1235insGT	NP_060245.3:n.*1234_*1235insGT
XM_017024801.2:c.994+2054_994+2055insGT	XP_016880290.2:n.994+2054_994+2055insGT
XM_017024802.2:c.994+2054_994+2055insGT	XP_016880291.2:n.994+2054_994+2055insGT
NM_017775.4:c.*1234_*1235insGT MANE Select	NP_060245.3:n.*1234_*1235insGT
NM_001271420.2:c.*1234_*1235insGT	NP_001258349.1:n.*1234_*1235insGT