Canonical Allele Identifier: CA2249869861

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027486G= , CM000679.2:g.16027486G=	GRCh38
NC_000017.10:g.15930800G= , CM000679.1:g.15930800G=	GRCh37
NC_000017.9:g.15871525G=	NCBI36
NG_029806.1:g.33107G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1107G= MANE Select	ENSP00000261647.5:p.Lys369=
ENST00000261647.9:c.1107G=	ENSP00000261647.5:p.Lys369=
ENST00000465567.1:n.1501G=
ENST00000470649.1:c.247+784G=	ENSP00000465627.1:n.247+784G=
ENST00000475723.5:c.1291G=
ENST00000481107.1:n.1775G=
ENST00000497842.6:n.1311G=
NM_001271420.1:c.786G=	NP_001258349.1:p.Lys262=
NM_017775.3:c.1107G=	NP_060245.3:p.Lys369=
XM_017024801.2:c.994+784G=	XP_016880290.2:n.994+784G=
XM_017024802.2:c.994+784G=	XP_016880291.2:n.994+784G=
NM_017775.4:c.1107G= MANE Select	NP_060245.3:p.Lys369=
NM_001271420.2:c.786G=	NP_001258349.1:p.Lys262=