Canonical Allele Identifier: CA2636264175

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028840-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028840_16028841insC , CM000679.2:g.16028840_16028841insC	GRCh38
NC_000017.10:g.15932154_15932155insC , CM000679.1:g.15932154_15932155insC	GRCh37
NC_000017.9:g.15872879_15872880insC	NCBI36
NG_029806.1:g.34461_34462insC
NG_047111.1:g.192906_192907insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1318_*1319insC MANE Select	ENSP00000261647.5:n.*1318_*1319insC
ENST00000261647.9:c.*1318_*1319insC	ENSP00000261647.5:n.*1318_*1319insC
ENST00000470649.1:c.247+2138_247+2139insC	ENSP00000465627.1:n.247+2138_247+2139insC
NM_001271420.1:c.*1318_*1319insC	NP_001258349.1:n.*1318_*1319insC
NM_017775.3:c.*1318_*1319insC	NP_060245.3:n.*1318_*1319insC
XM_017024801.2:c.994+2138_994+2139insC	XP_016880290.2:n.994+2138_994+2139insC
XM_017024802.2:c.994+2138_994+2139insC	XP_016880291.2:n.994+2138_994+2139insC
NM_017775.4:c.*1318_*1319insC MANE Select	NP_060245.3:n.*1318_*1319insC
NM_001271420.2:c.*1318_*1319insC	NP_001258349.1:n.*1318_*1319insC