Canonical Allele Identifier: CA2249869787

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027457A= , CM000679.2:g.16027457A=	GRCh38
NC_000017.10:g.15930771A= , CM000679.1:g.15930771A=	GRCh37
NC_000017.9:g.15871496A=	NCBI36
NG_029806.1:g.33078A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1078A= MANE Select	ENSP00000261647.5:p.Ile360=
ENST00000261647.9:c.1078A=	ENSP00000261647.5:p.Ile360=
ENST00000465567.1:n.1472A=
ENST00000470649.1:c.247+755A=	ENSP00000465627.1:n.247+755A=
ENST00000475723.5:c.1262A=
ENST00000481107.1:n.1746A=
ENST00000497842.6:n.1282A=
NM_001271420.1:c.757A=	NP_001258349.1:p.Ile253=
NM_017775.3:c.1078A=	NP_060245.3:p.Ile360=
XM_017024801.2:c.994+755A=	XP_016880290.2:n.994+755A=
XM_017024802.2:c.994+755A=	XP_016880291.2:n.994+755A=
NM_017775.4:c.1078A= MANE Select	NP_060245.3:p.Ile360=
NM_001271420.2:c.757A=	NP_001258349.1:p.Ile253=