Canonical Allele Identifier: CA2249871189

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028487G= , CM000679.2:g.16028487G=	GRCh38
NC_000017.10:g.15931801G= , CM000679.1:g.15931801G=	GRCh37
NC_000017.9:g.15872526G=	NCBI36
NG_029806.1:g.34108G=
NG_047111.1:g.193260C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*965G= MANE Select	ENSP00000261647.5:n.*965G=
ENST00000261647.9:c.*965G=	ENSP00000261647.5:n.*965G=
ENST00000465567.1:n.2502G=
ENST00000470649.1:c.247+1785G=	ENSP00000465627.1:n.247+1785G=
ENST00000475723.5:c.2292G=
ENST00000481107.1:n.2776G=
NM_001271420.1:c.*965G=	NP_001258349.1:n.*965G=
NM_017775.3:c.*965G=	NP_060245.3:n.*965G=
XM_017024801.2:c.994+1785G=	XP_016880290.2:n.994+1785G=
XM_017024802.2:c.994+1785G=	XP_016880291.2:n.994+1785G=
NM_017775.4:c.*965G= MANE Select	NP_060245.3:n.*965G=
NM_001271420.2:c.*965G=	NP_001258349.1:n.*965G=