Canonical Allele Identifier: CA2249821944

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16006458T= , CM000679.2:g.16006458T=	GRCh38
NC_000017.10:g.15909772T= , CM000679.1:g.15909772T=	GRCh37
NC_000017.9:g.15850497T=	NCBI36
NG_029806.1:g.12079T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.582-16T= MANE Select	ENSP00000261647.5:n.582-16T=
ENST00000261647.9:c.582-16T=	ENSP00000261647.5:n.582-16T=
ENST00000475723.5:c.766-16T=
ENST00000497842.6:n.692-16T=
NM_001271420.1:c.261-16T=	NP_001258349.1:n.261-16T=
NM_017775.3:c.582-16T=	NP_060245.3:n.582-16T=
XM_011523950.1:c.582-16T=	XP_011522252.1:n.582-16T=
XR_934261.1:n.1791+705A=
XM_017024801.2:c.582-16T=	XP_016880290.2:n.582-16T=
XM_017024802.2:c.582-16T=	XP_016880291.2:n.582-16T=
XM_024450814.1:c.582-16T=	XP_024306582.1:n.582-16T=
NM_017775.4:c.582-16T= MANE Select	NP_060245.3:n.582-16T=
NM_001271420.2:c.261-16T=	NP_001258349.1:n.261-16T=