Canonical Allele Identifier: CA2249814972

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999887C= , CM000679.2:g.15999887C=	GRCh38
NC_000017.10:g.15903201C= , CM000679.1:g.15903201C=	GRCh37
NC_000017.9:g.15843926C=	NCBI36
NG_029806.1:g.5508C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.39C= MANE Select	ENSP00000261647.5:p.Phe13=
ENST00000261647.9:c.39C=	ENSP00000261647.5:p.Phe13=
ENST00000466729.5:c.104C=
ENST00000470399.1:c.54C=	ENSP00000465082.1:p.Phe18=
ENST00000475723.5:c.86C=
ENST00000497842.6:n.64C=
ENST00000583704.1:n.64C=
NM_001271420.1:c.-420C=	NP_001258349.1:n.-420C=
NM_017775.3:c.39C=	NP_060245.3:p.Phe13=
XM_011523950.1:c.39C=	XP_011522252.1:p.Phe13=
XM_017024801.2:c.39C=	XP_016880290.2:p.Phe13=
XM_017024802.2:c.39C=	XP_016880291.2:p.Phe13=
XM_024450814.1:c.39C=	XP_024306582.1:p.Phe13=
NM_017775.4:c.39C= MANE Select	NP_060245.3:p.Phe13=
NM_001271420.2:c.-420C=	NP_001258349.1:n.-420C=