Canonical Allele Identifier: CA288164782

Gene: TTC19

Linked Data

• dbSNP Id: rs910507608
• gnomAD v4: 17-16027578-T-G
• MyVariant Identifiers: chr17:g.15930892T>G (hg19) ; chr17:g.16027578T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027578T>G , CM000679.2:g.16027578T>G	GRCh38
NC_000017.10:g.15930892T>G , CM000679.1:g.15930892T>G	GRCh37
NC_000017.9:g.15871617T>G	NCBI36
NG_029806.1:g.33199T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*56T>G MANE Select	ENSP00000261647.5:n.*56T>G
ENST00000261647.9:c.*56T>G	ENSP00000261647.5:n.*56T>G
ENST00000465567.1:n.1593T>G
ENST00000470649.1:c.247+876T>G	ENSP00000465627.1:n.247+876T>G
ENST00000475723.5:c.1383T>G
ENST00000481107.1:n.1867T>G
NM_001271420.1:c.*56T>G	NP_001258349.1:n.*56T>G
NM_017775.3:c.*56T>G	NP_060245.3:n.*56T>G
XM_017024801.2:c.994+876T>G	XP_016880290.2:n.994+876T>G
XM_017024802.2:c.994+876T>G	XP_016880291.2:n.994+876T>G
NM_017775.4:c.*56T>G MANE Select	NP_060245.3:n.*56T>G
NM_001271420.2:c.*56T>G	NP_001258349.1:n.*56T>G