Canonical Allele Identifier: CA2808599751

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027539_16027554dup , CM000679.2:g.16027539_16027554dup	GRCh38
NC_000017.10:g.15930853_15930868dup , CM000679.1:g.15930853_15930868dup	GRCh37
NC_000017.9:g.15871578_15871593dup	NCBI36
NG_029806.1:g.33160_33175dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*17_*32dup MANE Select	ENSP00000261647.5:n.*17_*32dup
ENST00000261647.9:c.*17_*32dup	ENSP00000261647.5:n.*17_*32dup
ENST00000465567.1:n.1554_1569dup
ENST00000470649.1:c.247+837_247+852dup	ENSP00000465627.1:n.247+837_247+852dup
ENST00000475723.5:c.1344_1359dup
ENST00000481107.1:n.1828_1843dup
NM_001271420.1:c.*17_*32dup	NP_001258349.1:n.*17_*32dup
NM_017775.3:c.*17_*32dup	NP_060245.3:n.*17_*32dup
XM_017024801.2:c.994+837_994+852dup	XP_016880290.2:n.994+837_994+852dup
XM_017024802.2:c.994+837_994+852dup	XP_016880291.2:n.994+837_994+852dup
NM_017775.4:c.*17_*32dup MANE Select	NP_060245.3:n.*17_*32dup
NM_001271420.2:c.*17_*32dup	NP_001258349.1:n.*17_*32dup