Canonical Allele Identifier: CA2249869900

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027519C= , CM000679.2:g.16027519C=	GRCh38
NC_000017.10:g.15930833C= , CM000679.1:g.15930833C=	GRCh37
NC_000017.9:g.15871558C=	NCBI36
NG_029806.1:g.33140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1140C= MANE Select	ENSP00000261647.5:p.Leu380=
ENST00000261647.9:c.1140C=	ENSP00000261647.5:p.Leu380=
ENST00000465567.1:n.1534C=
ENST00000470649.1:c.247+817C=	ENSP00000465627.1:n.247+817C=
ENST00000475723.5:c.1324C=
ENST00000481107.1:n.1808C=
ENST00000497842.6:n.1344C=
NM_001271420.1:c.819C=	NP_001258349.1:p.Leu273=
NM_017775.3:c.1140C=	NP_060245.3:p.Leu380=
XM_017024801.2:c.994+817C=	XP_016880290.2:n.994+817C=
XM_017024802.2:c.994+817C=	XP_016880291.2:n.994+817C=
NM_017775.4:c.1140C= MANE Select	NP_060245.3:p.Leu380=
NM_001271420.2:c.819C=	NP_001258349.1:p.Leu273=