Canonical Allele Identifier: CA2636264155

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028836-A-AAAAAAAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028843_16028844insCAAAAAAA , CM000679.2:g.16028843_16028844insCAAAAAAA	GRCh38
NC_000017.10:g.15932157_15932158insCAAAAAAA , CM000679.1:g.15932157_15932158insCAAAAAAA	GRCh37
NC_000017.9:g.15872882_15872883insCAAAAAAA	NCBI36
NG_029806.1:g.34464_34465insCAAAAAAA
NG_047111.1:g.192910_192911insGTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1321_*1322insCAAAAAAA MANE Select	ENSP00000261647.5:n.*1321_*1322insCAAAAAAA
ENST00000261647.9:c.*1321_*1322insCAAAAAAA	ENSP00000261647.5:n.*1321_*1322insCAAAAAAA
ENST00000470649.1:c.247+2141_247+2142insCAAAAAAA	ENSP00000465627.1:n.247+2141_247+2142insCAAAAAAA
NM_001271420.1:c.*1321_*1322insCAAAAAAA	NP_001258349.1:n.*1321_*1322insCAAAAAAA
NM_017775.3:c.*1321_*1322insCAAAAAAA	NP_060245.3:n.*1321_*1322insCAAAAAAA
XM_017024801.2:c.994+2141_994+2142insCAAAAAAA	XP_016880290.2:n.994+2141_994+2142insCAAAAAAA
XM_017024802.2:c.994+2141_994+2142insCAAAAAAA	XP_016880291.2:n.994+2141_994+2142insCAAAAAAA
NM_017775.4:c.*1321_*1322insCAAAAAAA MANE Select	NP_060245.3:n.*1321_*1322insCAAAAAAA
NM_001271420.2:c.*1321_*1322insCAAAAAAA	NP_001258349.1:n.*1321_*1322insCAAAAAAA