Canonical Allele Identifier: CA2249870834

Gene: TTC19

Linked Data

• dbSNP Id: rs1971649561

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028258dup , CM000679.2:g.16028258dup	GRCh38
NC_000017.10:g.15931572dup , CM000679.1:g.15931572dup	GRCh37
NC_000017.9:g.15872297dup	NCBI36
NG_029806.1:g.33879dup
NG_047111.1:g.193489dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*736dup MANE Select	ENSP00000261647.5:n.*736dup
ENST00000261647.9:c.*736dup	ENSP00000261647.5:n.*736dup
ENST00000465567.1:n.2273dup
ENST00000470649.1:c.247+1556dup	ENSP00000465627.1:n.247+1556dup
ENST00000475723.5:c.2063dup
ENST00000481107.1:n.2547dup
NM_001271420.1:c.*736dup	NP_001258349.1:n.*736dup
NM_017775.3:c.*736dup	NP_060245.3:n.*736dup
XM_017024801.2:c.994+1556dup	XP_016880290.2:n.994+1556dup
XM_017024802.2:c.994+1556dup	XP_016880291.2:n.994+1556dup
NM_017775.4:c.*736dup MANE Select	NP_060245.3:n.*736dup
NM_001271420.2:c.*736dup	NP_001258349.1:n.*736dup