Canonical Allele Identifier: CA2636262399

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027596-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027596C>G , CM000679.2:g.16027596C>G	GRCh38
NC_000017.10:g.15930910C>G , CM000679.1:g.15930910C>G	GRCh37
NC_000017.9:g.15871635C>G	NCBI36
NG_029806.1:g.33217C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*74C>G MANE Select	ENSP00000261647.5:n.*74C>G
ENST00000261647.9:c.*74C>G	ENSP00000261647.5:n.*74C>G
ENST00000465567.1:n.1611C>G
ENST00000470649.1:c.247+894C>G	ENSP00000465627.1:n.247+894C>G
ENST00000475723.5:c.1401C>G
ENST00000481107.1:n.1885C>G
NM_001271420.1:c.*74C>G	NP_001258349.1:n.*74C>G
NM_017775.3:c.*74C>G	NP_060245.3:n.*74C>G
XM_017024801.2:c.994+894C>G	XP_016880290.2:n.994+894C>G
XM_017024802.2:c.994+894C>G	XP_016880291.2:n.994+894C>G
NM_017775.4:c.*74C>G MANE Select	NP_060245.3:n.*74C>G
NM_001271420.2:c.*74C>G	NP_001258349.1:n.*74C>G