Canonical Allele Identifier: CA2636264153

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028835-A-AAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028837_16028838insCAA , CM000679.2:g.16028837_16028838insCAA	GRCh38
NC_000017.10:g.15932151_15932152insCAA , CM000679.1:g.15932151_15932152insCAA	GRCh37
NC_000017.9:g.15872876_15872877insCAA	NCBI36
NG_029806.1:g.34458_34459insCAA
NG_047111.1:g.192911_192912insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1315_*1316insCAA MANE Select	ENSP00000261647.5:n.*1315_*1316insCAA
ENST00000261647.9:c.*1315_*1316insCAA	ENSP00000261647.5:n.*1315_*1316insCAA
ENST00000470649.1:c.247+2135_247+2136insCAA	ENSP00000465627.1:n.247+2135_247+2136insCAA
NM_001271420.1:c.*1315_*1316insCAA	NP_001258349.1:n.*1315_*1316insCAA
NM_017775.3:c.*1315_*1316insCAA	NP_060245.3:n.*1315_*1316insCAA
XM_017024801.2:c.994+2135_994+2136insCAA	XP_016880290.2:n.994+2135_994+2136insCAA
XM_017024802.2:c.994+2135_994+2136insCAA	XP_016880291.2:n.994+2135_994+2136insCAA
NM_017775.4:c.*1315_*1316insCAA MANE Select	NP_060245.3:n.*1315_*1316insCAA
NM_001271420.2:c.*1315_*1316insCAA	NP_001258349.1:n.*1315_*1316insCAA