Canonical Allele Identifier: CA2249871110

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028446T= , CM000679.2:g.16028446T=	GRCh38
NC_000017.10:g.15931760T= , CM000679.1:g.15931760T=	GRCh37
NC_000017.9:g.15872485T=	NCBI36
NG_029806.1:g.34067T=
NG_047111.1:g.193301A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*924T= MANE Select	ENSP00000261647.5:n.*924T=
ENST00000261647.9:c.*924T=	ENSP00000261647.5:n.*924T=
ENST00000465567.1:n.2461T=
ENST00000470649.1:c.247+1744T=	ENSP00000465627.1:n.247+1744T=
ENST00000475723.5:c.2251T=
ENST00000481107.1:n.2735T=
NM_001271420.1:c.*924T=	NP_001258349.1:n.*924T=
NM_017775.3:c.*924T=	NP_060245.3:n.*924T=
XM_017024801.2:c.994+1744T=	XP_016880290.2:n.994+1744T=
XM_017024802.2:c.994+1744T=	XP_016880291.2:n.994+1744T=
NM_017775.4:c.*924T= MANE Select	NP_060245.3:n.*924T=
NM_001271420.2:c.*924T=	NP_001258349.1:n.*924T=