Canonical Allele Identifier: CA2249871739

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028753G= , CM000679.2:g.16028753G=	GRCh38
NC_000017.10:g.15932067G= , CM000679.1:g.15932067G=	GRCh37
NC_000017.9:g.15872792G=	NCBI36
NG_029806.1:g.34374G=
NG_047111.1:g.192994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1231G= MANE Select	ENSP00000261647.5:n.*1231G=
ENST00000261647.9:c.*1231G=	ENSP00000261647.5:n.*1231G=
ENST00000465567.1:n.2768G=
ENST00000470649.1:c.247+2051G=	ENSP00000465627.1:n.247+2051G=
ENST00000475723.5:c.2558G=
ENST00000481107.1:n.3042G=
NM_001271420.1:c.*1231G=	NP_001258349.1:n.*1231G=
NM_017775.3:c.*1231G=	NP_060245.3:n.*1231G=
XM_017024801.2:c.994+2051G=	XP_016880290.2:n.994+2051G=
XM_017024802.2:c.994+2051G=	XP_016880291.2:n.994+2051G=
NM_017775.4:c.*1231G= MANE Select	NP_060245.3:n.*1231G=
NM_001271420.2:c.*1231G=	NP_001258349.1:n.*1231G=