Canonical Allele Identifier: CA2249870639

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028115C= , CM000679.2:g.16028115C=	GRCh38
NC_000017.10:g.15931429C= , CM000679.1:g.15931429C=	GRCh37
NC_000017.9:g.15872154C=	NCBI36
NG_029806.1:g.33736C=
NG_047111.1:g.193632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*593C= MANE Select	ENSP00000261647.5:n.*593C=
ENST00000261647.9:c.*593C=	ENSP00000261647.5:n.*593C=
ENST00000465567.1:n.2130C=
ENST00000470649.1:c.247+1413C=	ENSP00000465627.1:n.247+1413C=
ENST00000475723.5:c.1920C=
ENST00000481107.1:n.2404C=
NM_001271420.1:c.*593C=	NP_001258349.1:n.*593C=
NM_017775.3:c.*593C=	NP_060245.3:n.*593C=
XM_017024801.2:c.994+1413C=	XP_016880290.2:n.994+1413C=
XM_017024802.2:c.994+1413C=	XP_016880291.2:n.994+1413C=
NM_017775.4:c.*593C= MANE Select	NP_060245.3:n.*593C=
NM_001271420.2:c.*593C=	NP_001258349.1:n.*593C=