Canonical Allele Identifier: CA2249870081

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027651T= , CM000679.2:g.16027651T=	GRCh38
NC_000017.10:g.15930965T= , CM000679.1:g.15930965T=	GRCh37
NC_000017.9:g.15871690T=	NCBI36
NG_029806.1:g.33272T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*129T= MANE Select	ENSP00000261647.5:n.*129T=
ENST00000261647.9:c.*129T=	ENSP00000261647.5:n.*129T=
ENST00000465567.1:n.1666T=
ENST00000470649.1:c.247+949T=	ENSP00000465627.1:n.247+949T=
ENST00000475723.5:c.1456T=
ENST00000481107.1:n.1940T=
NM_001271420.1:c.*129T=	NP_001258349.1:n.*129T=
NM_017775.3:c.*129T=	NP_060245.3:n.*129T=
XM_017024801.2:c.994+949T=	XP_016880290.2:n.994+949T=
XM_017024802.2:c.994+949T=	XP_016880291.2:n.994+949T=
NM_017775.4:c.*129T= MANE Select	NP_060245.3:n.*129T=
NM_001271420.2:c.*129T=	NP_001258349.1:n.*129T=