Canonical Allele Identifier: CA2249870110

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027688T= , CM000679.2:g.16027688T=	GRCh38
NC_000017.10:g.15931002T= , CM000679.1:g.15931002T=	GRCh37
NC_000017.9:g.15871727T=	NCBI36
NG_029806.1:g.33309T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*166T= MANE Select	ENSP00000261647.5:n.*166T=
ENST00000261647.9:c.*166T=	ENSP00000261647.5:n.*166T=
ENST00000465567.1:n.1703T=
ENST00000470649.1:c.247+986T=	ENSP00000465627.1:n.247+986T=
ENST00000475723.5:c.1493T=
ENST00000481107.1:n.1977T=
NM_001271420.1:c.*166T=	NP_001258349.1:n.*166T=
NM_017775.3:c.*166T=	NP_060245.3:n.*166T=
XM_017024801.2:c.994+986T=	XP_016880290.2:n.994+986T=
XM_017024802.2:c.994+986T=	XP_016880291.2:n.994+986T=
NM_017775.4:c.*166T= MANE Select	NP_060245.3:n.*166T=
NM_001271420.2:c.*166T=	NP_001258349.1:n.*166T=