Canonical Allele Identifier: CA981831917

Gene: TTC19

Linked Data

• dbSNP Id: rs1971656564
• gnomAD v3: 17-16028378-G-T
• gnomAD v4: 17-16028378-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028378G>T , CM000679.2:g.16028378G>T	GRCh38
NC_000017.10:g.15931692G>T , CM000679.1:g.15931692G>T	GRCh37
NC_000017.9:g.15872417G>T	NCBI36
NG_029806.1:g.33999G>T
NG_047111.1:g.193369C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*856G>T MANE Select	ENSP00000261647.5:n.*856G>T
ENST00000261647.9:c.*856G>T	ENSP00000261647.5:n.*856G>T
ENST00000465567.1:n.2393G>T
ENST00000470649.1:c.247+1676G>T	ENSP00000465627.1:n.247+1676G>T
ENST00000475723.5:c.2183G>T
ENST00000481107.1:n.2667G>T
NM_001271420.1:c.*856G>T	NP_001258349.1:n.*856G>T
NM_017775.3:c.*856G>T	NP_060245.3:n.*856G>T
XM_017024801.2:c.994+1676G>T	XP_016880290.2:n.994+1676G>T
XM_017024802.2:c.994+1676G>T	XP_016880291.2:n.994+1676G>T
NM_017775.4:c.*856G>T MANE Select	NP_060245.3:n.*856G>T
NM_001271420.2:c.*856G>T	NP_001258349.1:n.*856G>T