Canonical Allele Identifier: CA624957402

Gene: TTC19

Linked Data

• dbSNP Id: rs1339211875
• gnomAD v2: 17-15930915-A-G
• gnomAD v4: 17-16027601-A-G
• MyVariant Identifiers: chr17:g.15930915A>G (hg19) ; chr17:g.16027601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027601A>G , CM000679.2:g.16027601A>G	GRCh38
NC_000017.10:g.15930915A>G , CM000679.1:g.15930915A>G	GRCh37
NC_000017.9:g.15871640A>G	NCBI36
NG_029806.1:g.33222A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*79A>G MANE Select	ENSP00000261647.5:n.*79A>G
ENST00000261647.9:c.*79A>G	ENSP00000261647.5:n.*79A>G
ENST00000465567.1:n.1616A>G
ENST00000470649.1:c.247+899A>G	ENSP00000465627.1:n.247+899A>G
ENST00000475723.5:c.1406A>G
ENST00000481107.1:n.1890A>G
NM_001271420.1:c.*79A>G	NP_001258349.1:n.*79A>G
NM_017775.3:c.*79A>G	NP_060245.3:n.*79A>G
XM_017024801.2:c.994+899A>G	XP_016880290.2:n.994+899A>G
XM_017024802.2:c.994+899A>G	XP_016880291.2:n.994+899A>G
NM_017775.4:c.*79A>G MANE Select	NP_060245.3:n.*79A>G
NM_001271420.2:c.*79A>G	NP_001258349.1:n.*79A>G