Canonical Allele Identifier: CA2249871058

Gene: TTC19

Linked Data

• dbSNP Id: rs1597474388

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028403T>A , CM000679.2:g.16028403T>A	GRCh38
NC_000017.10:g.15931717T>A , CM000679.1:g.15931717T>A	GRCh37
NC_000017.9:g.15872442T>A	NCBI36
NG_029806.1:g.34024T>A
NG_047111.1:g.193344A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*881T>A MANE Select	ENSP00000261647.5:n.*881T>A
ENST00000261647.9:c.*881T>A	ENSP00000261647.5:n.*881T>A
ENST00000465567.1:n.2418T>A
ENST00000470649.1:c.247+1701T>A	ENSP00000465627.1:n.247+1701T>A
ENST00000475723.5:c.2208T>A
ENST00000481107.1:n.2692T>A
NM_001271420.1:c.*881T>A	NP_001258349.1:n.*881T>A
NM_017775.3:c.*881T>A	NP_060245.3:n.*881T>A
XM_017024801.2:c.994+1701T>A	XP_016880290.2:n.994+1701T>A
XM_017024802.2:c.994+1701T>A	XP_016880291.2:n.994+1701T>A
NM_017775.4:c.*881T>A MANE Select	NP_060245.3:n.*881T>A
NM_001271420.2:c.*881T>A	NP_001258349.1:n.*881T>A