Canonical Allele Identifier: CA2249869838

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027480G= , CM000679.2:g.16027480G=	GRCh38
NC_000017.10:g.15930794G= , CM000679.1:g.15930794G=	GRCh37
NC_000017.9:g.15871519G=	NCBI36
NG_029806.1:g.33101G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1101G= MANE Select	ENSP00000261647.5:p.Leu367=
ENST00000261647.9:c.1101G=	ENSP00000261647.5:p.Leu367=
ENST00000465567.1:n.1495G=
ENST00000470649.1:c.247+778G=	ENSP00000465627.1:n.247+778G=
ENST00000475723.5:c.1285G=
ENST00000481107.1:n.1769G=
ENST00000497842.6:n.1305G=
NM_001271420.1:c.780G=	NP_001258349.1:p.Leu260=
NM_017775.3:c.1101G=	NP_060245.3:p.Leu367=
XM_017024801.2:c.994+778G=	XP_016880290.2:n.994+778G=
XM_017024802.2:c.994+778G=	XP_016880291.2:n.994+778G=
NM_017775.4:c.1101G= MANE Select	NP_060245.3:p.Leu367=
NM_001271420.2:c.780G=	NP_001258349.1:p.Leu260=