Canonical Allele Identifier: CA2249869781

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027456_16027458delinsCAT , CM000679.2:g.16027456_16027458delinsCAT	GRCh38
NC_000017.10:g.15930770_15930772delinsCAT , CM000679.1:g.15930770_15930772delinsCAT	GRCh37
NC_000017.9:g.15871495_15871497delinsCAT	NCBI36
NG_029806.1:g.33077_33079delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1077_1079delinsCAT MANE Select	ENSP00000261647.5:p.His359=
ENST00000261647.9:c.1077_1079delinsCAT	ENSP00000261647.5:p.His359=
ENST00000465567.1:n.1471_1473delinsCAT
ENST00000470649.1:c.247+754_247+756delinsCAT	ENSP00000465627.1:n.247+754_247+756delinsCAT
ENST00000475723.5:c.1261_1263delinsCAT
ENST00000481107.1:n.1745_1747delinsCAT
ENST00000497842.6:n.1281_1283delinsCAT
NM_001271420.1:c.756_758delinsCAT	NP_001258349.1:p.His252=
NM_017775.3:c.1077_1079delinsCAT	NP_060245.3:p.His359=
XM_017024801.2:c.994+754_994+756delinsCAT	XP_016880290.2:n.994+754_994+756delinsCAT
XM_017024802.2:c.994+754_994+756delinsCAT	XP_016880291.2:n.994+754_994+756delinsCAT
NM_017775.4:c.1077_1079delinsCAT MANE Select	NP_060245.3:p.His359=
NM_001271420.2:c.756_758delinsCAT	NP_001258349.1:p.His252=