Canonical Allele Identifier: CA2249869934

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027542_16027543delinsGA , CM000679.2:g.16027542_16027543delinsGA	GRCh38
NC_000017.10:g.15930856_15930857delinsGA , CM000679.1:g.15930856_15930857delinsGA	GRCh37
NC_000017.9:g.15871581_15871582delinsGA	NCBI36
NG_029806.1:g.33163_33164delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*20_*21delinsGA MANE Select	ENSP00000261647.5:n.*20_*21delinsGA
ENST00000261647.9:c.*20_*21delinsGA	ENSP00000261647.5:n.*20_*21delinsGA
ENST00000465567.1:n.1557_1558delinsGA
ENST00000470649.1:c.247+840_247+841delinsGA	ENSP00000465627.1:n.247+840_247+841delinsGA
ENST00000475723.5:c.1347_1348delinsGA
ENST00000481107.1:n.1831_1832delinsGA
NM_001271420.1:c.*20_*21delinsGA	NP_001258349.1:n.*20_*21delinsGA
NM_017775.3:c.*20_*21delinsGA	NP_060245.3:n.*20_*21delinsGA
XM_017024801.2:c.994+840_994+841delinsGA	XP_016880290.2:n.994+840_994+841delinsGA
XM_017024802.2:c.994+840_994+841delinsGA	XP_016880291.2:n.994+840_994+841delinsGA
NM_017775.4:c.*20_*21delinsGA MANE Select	NP_060245.3:n.*20_*21delinsGA
NM_001271420.2:c.*20_*21delinsGA	NP_001258349.1:n.*20_*21delinsGA