Canonical Allele Identifier: CA2249870805

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028229T= , CM000679.2:g.16028229T=	GRCh38
NC_000017.10:g.15931543T= , CM000679.1:g.15931543T=	GRCh37
NC_000017.9:g.15872268T=	NCBI36
NG_029806.1:g.33850T=
NG_047111.1:g.193518A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*707T= MANE Select	ENSP00000261647.5:n.*707T=
ENST00000261647.9:c.*707T=	ENSP00000261647.5:n.*707T=
ENST00000465567.1:n.2244T=
ENST00000470649.1:c.247+1527T=	ENSP00000465627.1:n.247+1527T=
ENST00000475723.5:c.2034T=
ENST00000481107.1:n.2518T=
NM_001271420.1:c.*707T=	NP_001258349.1:n.*707T=
NM_017775.3:c.*707T=	NP_060245.3:n.*707T=
XM_017024801.2:c.994+1527T=	XP_016880290.2:n.994+1527T=
XM_017024802.2:c.994+1527T=	XP_016880291.2:n.994+1527T=
NM_017775.4:c.*707T= MANE Select	NP_060245.3:n.*707T=
NM_001271420.2:c.*707T=	NP_001258349.1:n.*707T=