Canonical Allele Identifier: CA2249814978

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999899G= , CM000679.2:g.15999899G=	GRCh38
NC_000017.10:g.15903213G= , CM000679.1:g.15903213G=	GRCh37
NC_000017.9:g.15843938G=	NCBI36
NG_029806.1:g.5520G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.51G= MANE Select	ENSP00000261647.5:p.Ala17=
ENST00000261647.9:c.51G=	ENSP00000261647.5:p.Ala17=
ENST00000466729.5:c.116G=
ENST00000470399.1:c.66G=	ENSP00000465082.1:p.Ala22=
ENST00000475723.5:c.98G=
ENST00000497842.6:n.76G=
ENST00000583704.1:n.76G=
NM_001271420.1:c.-408G=	NP_001258349.1:n.-408G=
NM_017775.3:c.51G=	NP_060245.3:p.Ala17=
XM_011523950.1:c.51G=	XP_011522252.1:p.Ala17=
XM_017024801.2:c.51G=	XP_016880290.2:p.Ala17=
XM_017024802.2:c.51G=	XP_016880291.2:p.Ala17=
XM_024450814.1:c.51G=	XP_024306582.1:p.Ala17=
NM_017775.4:c.51G= MANE Select	NP_060245.3:p.Ala17=
NM_001271420.2:c.-408G=	NP_001258349.1:n.-408G=