Canonical Allele Identifier: CA2636262392

Gene: TTC19

Linked Data

• gnomAD v4: 17-16027572-T-TATC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027575_16027577dup , CM000679.2:g.16027575_16027577dup	GRCh38
NC_000017.10:g.15930889_15930891dup , CM000679.1:g.15930889_15930891dup	GRCh37
NC_000017.9:g.15871614_15871616dup	NCBI36
NG_029806.1:g.33196_33198dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*53_*55dup MANE Select	ENSP00000261647.5:n.*53_*55dup
ENST00000261647.9:c.*53_*55dup	ENSP00000261647.5:n.*53_*55dup
ENST00000465567.1:n.1590_1592dup
ENST00000470649.1:c.247+873_247+875dup	ENSP00000465627.1:n.247+873_247+875dup
ENST00000475723.5:c.1380_1382dup
ENST00000481107.1:n.1864_1866dup
NM_001271420.1:c.*53_*55dup	NP_001258349.1:n.*53_*55dup
NM_017775.3:c.*53_*55dup	NP_060245.3:n.*53_*55dup
XM_017024801.2:c.994+873_994+875dup	XP_016880290.2:n.994+873_994+875dup
XM_017024802.2:c.994+873_994+875dup	XP_016880291.2:n.994+873_994+875dup
NM_017775.4:c.*53_*55dup MANE Select	NP_060245.3:n.*53_*55dup
NM_001271420.2:c.*53_*55dup	NP_001258349.1:n.*53_*55dup