Canonical Allele Identifier: CA726463917

Gene: TTC19

Linked Data

• dbSNP Id: rs1375702209
• gnomAD v4: 17-16028221-C-G
• MyVariant Identifiers: chr17:g.15931535C>G (hg19) ; chr17:g.16028221C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028221C>G , CM000679.2:g.16028221C>G	GRCh38
NC_000017.10:g.15931535C>G , CM000679.1:g.15931535C>G	GRCh37
NC_000017.9:g.15872260C>G	NCBI36
NG_029806.1:g.33842C>G
NG_047111.1:g.193526G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*699C>G MANE Select	ENSP00000261647.5:n.*699C>G
ENST00000261647.9:c.*699C>G	ENSP00000261647.5:n.*699C>G
ENST00000465567.1:n.2236C>G
ENST00000470649.1:c.247+1519C>G	ENSP00000465627.1:n.247+1519C>G
ENST00000475723.5:c.2026C>G
ENST00000481107.1:n.2510C>G
NM_001271420.1:c.*699C>G	NP_001258349.1:n.*699C>G
NM_017775.3:c.*699C>G	NP_060245.3:n.*699C>G
XM_017024801.2:c.994+1519C>G	XP_016880290.2:n.994+1519C>G
XM_017024802.2:c.994+1519C>G	XP_016880291.2:n.994+1519C>G
NM_017775.4:c.*699C>G MANE Select	NP_060245.3:n.*699C>G
NM_001271420.2:c.*699C>G	NP_001258349.1:n.*699C>G