Canonical Allele Identifier: CA2249814917

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999813G= , CM000679.2:g.15999813G=	GRCh38
NC_000017.10:g.15903127G= , CM000679.1:g.15903127G=	GRCh37
NC_000017.9:g.15843852G=	NCBI36
NG_029806.1:g.5434G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-36G=	ENSP00000261647.5:n.-36G=
ENST00000466729.5:c.30G=
ENST00000475723.5:c.12G=
NM_001271420.1:c.-494G=	NP_001258349.1:n.-494G=
NM_017775.3:c.-36G=	NP_060245.3:n.-36G=
XM_011523950.1:c.-36G=	XP_011522252.1:n.-36G=
XM_017024801.2:c.-36G=	XP_016880290.2:n.-36G=
XM_017024802.2:c.-36G=	XP_016880291.2:n.-36G=
XM_024450814.1:c.-36G=	XP_024306582.1:n.-36G=