Canonical Allele Identifier: CA2510782709

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028350_16028351insTTT , CM000679.2:g.16028350_16028351insTTT	GRCh38
NC_000017.10:g.15931664_15931665insTTT , CM000679.1:g.15931664_15931665insTTT	GRCh37
NC_000017.9:g.15872389_15872390insTTT	NCBI36
NG_029806.1:g.33971_33972insTTT
NG_047111.1:g.193396_193397insAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*828_*829insTTT MANE Select	ENSP00000261647.5:n.*828_*829insTTT
ENST00000261647.9:c.*828_*829insTTT	ENSP00000261647.5:n.*828_*829insTTT
ENST00000465567.1:n.2365_2366insTTT
ENST00000470649.1:c.247+1648_247+1649insTTT	ENSP00000465627.1:n.247+1648_247+1649insTTT
ENST00000475723.5:c.2155_2156insTTT
ENST00000481107.1:n.2639_2640insTTT
NM_001271420.1:c.*828_*829insTTT	NP_001258349.1:n.*828_*829insTTT
NM_017775.3:c.*828_*829insTTT	NP_060245.3:n.*828_*829insTTT
XM_017024801.2:c.994+1648_994+1649insTTT	XP_016880290.2:n.994+1648_994+1649insTTT
XM_017024802.2:c.994+1648_994+1649insTTT	XP_016880291.2:n.994+1648_994+1649insTTT
NM_017775.4:c.*828_*829insTTT MANE Select	NP_060245.3:n.*828_*829insTTT
NM_001271420.2:c.*828_*829insTTT	NP_001258349.1:n.*828_*829insTTT