Canonical Allele Identifier: CA2636262426

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027657-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027659dup , CM000679.2:g.16027659dup	GRCh38
NC_000017.10:g.15930973dup , CM000679.1:g.15930973dup	GRCh37
NC_000017.9:g.15871698dup	NCBI36
NG_029806.1:g.33280dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*137dup MANE Select	ENSP00000261647.5:n.*137dup
ENST00000261647.9:c.*137dup	ENSP00000261647.5:n.*137dup
ENST00000465567.1:n.1674dup
ENST00000470649.1:c.247+957dup	ENSP00000465627.1:n.247+957dup
ENST00000475723.5:c.1464dup
ENST00000481107.1:n.1948dup
NM_001271420.1:c.*137dup	NP_001258349.1:n.*137dup
NM_017775.3:c.*137dup	NP_060245.3:n.*137dup
XM_017024801.2:c.994+957dup	XP_016880290.2:n.994+957dup
XM_017024802.2:c.994+957dup	XP_016880291.2:n.994+957dup
NM_017775.4:c.*137dup MANE Select	NP_060245.3:n.*137dup
NM_001271420.2:c.*137dup	NP_001258349.1:n.*137dup