Canonical Allele Identifier: CA2249870027

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027601A= , CM000679.2:g.16027601A=	GRCh38
NC_000017.10:g.15930915A= , CM000679.1:g.15930915A=	GRCh37
NC_000017.9:g.15871640A=	NCBI36
NG_029806.1:g.33222A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*79A= MANE Select	ENSP00000261647.5:n.*79A=
ENST00000261647.9:c.*79A=	ENSP00000261647.5:n.*79A=
ENST00000465567.1:n.1616A=
ENST00000470649.1:c.247+899A=	ENSP00000465627.1:n.247+899A=
ENST00000475723.5:c.1406A=
ENST00000481107.1:n.1890A=
NM_001271420.1:c.*79A=	NP_001258349.1:n.*79A=
NM_017775.3:c.*79A=	NP_060245.3:n.*79A=
XM_017024801.2:c.994+899A=	XP_016880290.2:n.994+899A=
XM_017024802.2:c.994+899A=	XP_016880291.2:n.994+899A=
NM_017775.4:c.*79A= MANE Select	NP_060245.3:n.*79A=
NM_001271420.2:c.*79A=	NP_001258349.1:n.*79A=