Canonical Allele Identifier: CA2249870981

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028370G= , CM000679.2:g.16028370G=	GRCh38
NC_000017.10:g.15931684G= , CM000679.1:g.15931684G=	GRCh37
NC_000017.9:g.15872409G=	NCBI36
NG_029806.1:g.33991G=
NG_047111.1:g.193377C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*848G= MANE Select	ENSP00000261647.5:n.*848G=
ENST00000261647.9:c.*848G=	ENSP00000261647.5:n.*848G=
ENST00000465567.1:n.2385G=
ENST00000470649.1:c.247+1668G=	ENSP00000465627.1:n.247+1668G=
ENST00000475723.5:c.2175G=
ENST00000481107.1:n.2659G=
NM_001271420.1:c.*848G=	NP_001258349.1:n.*848G=
NM_017775.3:c.*848G=	NP_060245.3:n.*848G=
XM_017024801.2:c.994+1668G=	XP_016880290.2:n.994+1668G=
XM_017024802.2:c.994+1668G=	XP_016880291.2:n.994+1668G=
NM_017775.4:c.*848G= MANE Select	NP_060245.3:n.*848G=
NM_001271420.2:c.*848G=	NP_001258349.1:n.*848G=