Canonical Allele Identifier: CA2249870068

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027633G= , CM000679.2:g.16027633G=	GRCh38
NC_000017.10:g.15930947G= , CM000679.1:g.15930947G=	GRCh37
NC_000017.9:g.15871672G=	NCBI36
NG_029806.1:g.33254G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*111G= MANE Select	ENSP00000261647.5:n.*111G=
ENST00000261647.9:c.*111G=	ENSP00000261647.5:n.*111G=
ENST00000465567.1:n.1648G=
ENST00000470649.1:c.247+931G=	ENSP00000465627.1:n.247+931G=
ENST00000475723.5:c.1438G=
ENST00000481107.1:n.1922G=
NM_001271420.1:c.*111G=	NP_001258349.1:n.*111G=
NM_017775.3:c.*111G=	NP_060245.3:n.*111G=
XM_017024801.2:c.994+931G=	XP_016880290.2:n.994+931G=
XM_017024802.2:c.994+931G=	XP_016880291.2:n.994+931G=
NM_017775.4:c.*111G= MANE Select	NP_060245.3:n.*111G=
NM_001271420.2:c.*111G=	NP_001258349.1:n.*111G=