Canonical Allele Identifier: CA2249870112

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027692A= , CM000679.2:g.16027692A=	GRCh38
NC_000017.10:g.15931006A= , CM000679.1:g.15931006A=	GRCh37
NC_000017.9:g.15871731A=	NCBI36
NG_029806.1:g.33313A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*170A= MANE Select	ENSP00000261647.5:n.*170A=
ENST00000261647.9:c.*170A=	ENSP00000261647.5:n.*170A=
ENST00000465567.1:n.1707A=
ENST00000470649.1:c.247+990A=	ENSP00000465627.1:n.247+990A=
ENST00000475723.5:c.1497A=
ENST00000481107.1:n.1981A=
NM_001271420.1:c.*170A=	NP_001258349.1:n.*170A=
NM_017775.3:c.*170A=	NP_060245.3:n.*170A=
XM_017024801.2:c.994+990A=	XP_016880290.2:n.994+990A=
XM_017024802.2:c.994+990A=	XP_016880291.2:n.994+990A=
NM_017775.4:c.*170A= MANE Select	NP_060245.3:n.*170A=
NM_001271420.2:c.*170A=	NP_001258349.1:n.*170A=