Canonical Allele Identifier: CA2249870811

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028231T= , CM000679.2:g.16028231T=	GRCh38
NC_000017.10:g.15931545T= , CM000679.1:g.15931545T=	GRCh37
NC_000017.9:g.15872270T=	NCBI36
NG_029806.1:g.33852T=
NG_047111.1:g.193516A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*709T= MANE Select	ENSP00000261647.5:n.*709T=
ENST00000261647.9:c.*709T=	ENSP00000261647.5:n.*709T=
ENST00000465567.1:n.2246T=
ENST00000470649.1:c.247+1529T=	ENSP00000465627.1:n.247+1529T=
ENST00000475723.5:c.2036T=
ENST00000481107.1:n.2520T=
NM_001271420.1:c.*709T=	NP_001258349.1:n.*709T=
NM_017775.3:c.*709T=	NP_060245.3:n.*709T=
XM_017024801.2:c.994+1529T=	XP_016880290.2:n.994+1529T=
XM_017024802.2:c.994+1529T=	XP_016880291.2:n.994+1529T=
NM_017775.4:c.*709T= MANE Select	NP_060245.3:n.*709T=
NM_001271420.2:c.*709T=	NP_001258349.1:n.*709T=