Canonical Allele Identifier: CA2507951135

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028507del , CM000679.2:g.16028507del	GRCh38
NC_000017.10:g.15931821del , CM000679.1:g.15931821del	GRCh37
NC_000017.9:g.15872546del	NCBI36
NG_029806.1:g.34128del
NG_047111.1:g.193240del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*985del MANE Select	ENSP00000261647.5:n.*985del
ENST00000261647.9:c.*985del	ENSP00000261647.5:n.*985del
ENST00000465567.1:n.2522del
ENST00000470649.1:c.247+1805del	ENSP00000465627.1:n.247+1805del
ENST00000475723.5:c.2312del
ENST00000481107.1:n.2796del
NM_001271420.1:c.*985del	NP_001258349.1:n.*985del
NM_017775.3:c.*985del	NP_060245.3:n.*985del
XM_017024801.2:c.994+1805del	XP_016880290.2:n.994+1805del
XM_017024802.2:c.994+1805del	XP_016880291.2:n.994+1805del
NM_017775.4:c.*985del MANE Select	NP_060245.3:n.*985del
NM_001271420.2:c.*985del	NP_001258349.1:n.*985del