Canonical Allele Identifier: CA2249870765

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028192_16028194delinsTAA , CM000679.2:g.16028192_16028194delinsTAA	GRCh38
NC_000017.10:g.15931506_15931508delinsTAA , CM000679.1:g.15931506_15931508delinsTAA	GRCh37
NC_000017.9:g.15872231_15872233delinsTAA	NCBI36
NG_029806.1:g.33813_33815delinsTAA
NG_047111.1:g.193553_193555delinsTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*670_*672delinsTAA MANE Select	ENSP00000261647.5:n.*670_*672delinsTAA
ENST00000261647.9:c.*670_*672delinsTAA	ENSP00000261647.5:n.*670_*672delinsTAA
ENST00000465567.1:n.2207_2209delinsTAA
ENST00000470649.1:c.247+1490_247+1492delinsTAA	ENSP00000465627.1:n.247+1490_247+1492delinsTAA
ENST00000475723.5:c.1997_1999delinsTAA
ENST00000481107.1:n.2481_2483delinsTAA
NM_001271420.1:c.*670_*672delinsTAA	NP_001258349.1:n.*670_*672delinsTAA
NM_017775.3:c.*670_*672delinsTAA	NP_060245.3:n.*670_*672delinsTAA
XM_017024801.2:c.994+1490_994+1492delinsTAA	XP_016880290.2:n.994+1490_994+1492delinsTAA
XM_017024802.2:c.994+1490_994+1492delinsTAA	XP_016880291.2:n.994+1490_994+1492delinsTAA
NM_017775.4:c.*670_*672delinsTAA MANE Select	NP_060245.3:n.*670_*672delinsTAA
NM_001271420.2:c.*670_*672delinsTAA	NP_001258349.1:n.*670_*672delinsTAA