Canonical Allele Identifier: CA2249869950

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027556A= , CM000679.2:g.16027556A=	GRCh38
NC_000017.10:g.15930870A= , CM000679.1:g.15930870A=	GRCh37
NC_000017.9:g.15871595A=	NCBI36
NG_029806.1:g.33177A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*34A= MANE Select	ENSP00000261647.5:n.*34A=
ENST00000261647.9:c.*34A=	ENSP00000261647.5:n.*34A=
ENST00000465567.1:n.1571A=
ENST00000470649.1:c.247+854A=	ENSP00000465627.1:n.247+854A=
ENST00000475723.5:c.1361A=
ENST00000481107.1:n.1845A=
NM_001271420.1:c.*34A=	NP_001258349.1:n.*34A=
NM_017775.3:c.*34A=	NP_060245.3:n.*34A=
XM_017024801.2:c.994+854A=	XP_016880290.2:n.994+854A=
XM_017024802.2:c.994+854A=	XP_016880291.2:n.994+854A=
NM_017775.4:c.*34A= MANE Select	NP_060245.3:n.*34A=
NM_001271420.2:c.*34A=	NP_001258349.1:n.*34A=