Canonical Allele Identifier: CA2249869885

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027499T= , CM000679.2:g.16027499T=	GRCh38
NC_000017.10:g.15930813T= , CM000679.1:g.15930813T=	GRCh37
NC_000017.9:g.15871538T=	NCBI36
NG_029806.1:g.33120T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1120T= MANE Select	ENSP00000261647.5:p.Leu374=
ENST00000261647.9:c.1120T=	ENSP00000261647.5:p.Leu374=
ENST00000465567.1:n.1514T=
ENST00000470649.1:c.247+797T=	ENSP00000465627.1:n.247+797T=
ENST00000475723.5:c.1304T=
ENST00000481107.1:n.1788T=
ENST00000497842.6:n.1324T=
NM_001271420.1:c.799T=	NP_001258349.1:p.Leu267=
NM_017775.3:c.1120T=	NP_060245.3:p.Leu374=
XM_017024801.2:c.994+797T=	XP_016880290.2:n.994+797T=
XM_017024802.2:c.994+797T=	XP_016880291.2:n.994+797T=
NM_017775.4:c.1120T= MANE Select	NP_060245.3:p.Leu374=
NM_001271420.2:c.799T=	NP_001258349.1:p.Leu267=