Canonical Allele Identifier: CA2249870102

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027674C= , CM000679.2:g.16027674C=	GRCh38
NC_000017.10:g.15930988C= , CM000679.1:g.15930988C=	GRCh37
NC_000017.9:g.15871713C=	NCBI36
NG_029806.1:g.33295C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*152C= MANE Select	ENSP00000261647.5:n.*152C=
ENST00000261647.9:c.*152C=	ENSP00000261647.5:n.*152C=
ENST00000465567.1:n.1689C=
ENST00000470649.1:c.247+972C=	ENSP00000465627.1:n.247+972C=
ENST00000475723.5:c.1479C=
ENST00000481107.1:n.1963C=
NM_001271420.1:c.*152C=	NP_001258349.1:n.*152C=
NM_017775.3:c.*152C=	NP_060245.3:n.*152C=
XM_017024801.2:c.994+972C=	XP_016880290.2:n.994+972C=
XM_017024802.2:c.994+972C=	XP_016880291.2:n.994+972C=
NM_017775.4:c.*152C= MANE Select	NP_060245.3:n.*152C=
NM_001271420.2:c.*152C=	NP_001258349.1:n.*152C=