Canonical Allele Identifier: CA2249871006

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028385C= , CM000679.2:g.16028385C=	GRCh38
NC_000017.10:g.15931699C= , CM000679.1:g.15931699C=	GRCh37
NC_000017.9:g.15872424C=	NCBI36
NG_029806.1:g.34006C=
NG_047111.1:g.193362G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*863C= MANE Select	ENSP00000261647.5:n.*863C=
ENST00000261647.9:c.*863C=	ENSP00000261647.5:n.*863C=
ENST00000465567.1:n.2400C=
ENST00000470649.1:c.247+1683C=	ENSP00000465627.1:n.247+1683C=
ENST00000475723.5:c.2190C=
ENST00000481107.1:n.2674C=
NM_001271420.1:c.*863C=	NP_001258349.1:n.*863C=
NM_017775.3:c.*863C=	NP_060245.3:n.*863C=
XM_017024801.2:c.994+1683C=	XP_016880290.2:n.994+1683C=
XM_017024802.2:c.994+1683C=	XP_016880291.2:n.994+1683C=
NM_017775.4:c.*863C= MANE Select	NP_060245.3:n.*863C=
NM_001271420.2:c.*863C=	NP_001258349.1:n.*863C=