Canonical Allele Identifier: CA2249814890

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999788G= , CM000679.2:g.15999788G=	GRCh38
NC_000017.10:g.15903102G= , CM000679.1:g.15903102G=	GRCh37
NC_000017.9:g.15843827G=	NCBI36
NG_029806.1:g.5409G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-61G=	ENSP00000261647.5:n.-61G=
ENST00000466729.5:c.5G=
NM_001271420.1:c.-519G=	NP_001258349.1:n.-519G=
NM_017775.3:c.-61G=	NP_060245.3:n.-61G=
XM_011523950.1:c.-61G=	XP_011522252.1:n.-61G=
XM_017024801.2:c.-61G=	XP_016880290.2:n.-61G=
XM_017024802.2:c.-61G=	XP_016880291.2:n.-61G=
XM_024450814.1:c.-61G=	XP_024306582.1:n.-61G=