Canonical Allele Identifier: CA2249870835

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028263C= , CM000679.2:g.16028263C=	GRCh38
NC_000017.10:g.15931577C= , CM000679.1:g.15931577C=	GRCh37
NC_000017.9:g.15872302C=	NCBI36
NG_029806.1:g.33884C=
NG_047111.1:g.193484G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*741C= MANE Select	ENSP00000261647.5:n.*741C=
ENST00000261647.9:c.*741C=	ENSP00000261647.5:n.*741C=
ENST00000465567.1:n.2278C=
ENST00000470649.1:c.247+1561C=	ENSP00000465627.1:n.247+1561C=
ENST00000475723.5:c.2068C=
ENST00000481107.1:n.2552C=
NM_001271420.1:c.*741C=	NP_001258349.1:n.*741C=
NM_017775.3:c.*741C=	NP_060245.3:n.*741C=
XM_017024801.2:c.994+1561C=	XP_016880290.2:n.994+1561C=
XM_017024802.2:c.994+1561C=	XP_016880291.2:n.994+1561C=
NM_017775.4:c.*741C= MANE Select	NP_060245.3:n.*741C=
NM_001271420.2:c.*741C=	NP_001258349.1:n.*741C=