Canonical Allele Identifier: CA981831567

Gene: TTC19

Linked Data

• dbSNP Id: rs1971608692
• gnomAD v3: 17-16027542-G-A
• gnomAD v4: 17-16027542-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027542G>A , CM000679.2:g.16027542G>A	GRCh38
NC_000017.10:g.15930856G>A , CM000679.1:g.15930856G>A	GRCh37
NC_000017.9:g.15871581G>A	NCBI36
NG_029806.1:g.33163G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*20G>A MANE Select	ENSP00000261647.5:n.*20G>A
ENST00000261647.9:c.*20G>A	ENSP00000261647.5:n.*20G>A
ENST00000465567.1:n.1557G>A
ENST00000470649.1:c.247+840G>A	ENSP00000465627.1:n.247+840G>A
ENST00000475723.5:c.1347G>A
ENST00000481107.1:n.1831G>A
NM_001271420.1:c.*20G>A	NP_001258349.1:n.*20G>A
NM_017775.3:c.*20G>A	NP_060245.3:n.*20G>A
XM_017024801.2:c.994+840G>A	XP_016880290.2:n.994+840G>A
XM_017024802.2:c.994+840G>A	XP_016880291.2:n.994+840G>A
NM_017775.4:c.*20G>A MANE Select	NP_060245.3:n.*20G>A
NM_001271420.2:c.*20G>A	NP_001258349.1:n.*20G>A