Canonical Allele Identifier: CA2249872565

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028902A= , CM000679.2:g.16028902A=	GRCh38
NC_000017.10:g.15932216A= , CM000679.1:g.15932216A=	GRCh37
NC_000017.9:g.15872941A=	NCBI36
NG_029806.1:g.34523A=
NG_047111.1:g.192845T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1380A= MANE Select	ENSP00000261647.5:n.*1380A=
ENST00000261647.9:c.*1380A=	ENSP00000261647.5:n.*1380A=
ENST00000470649.1:c.247+2200A=	ENSP00000465627.1:n.247+2200A=
NM_001271420.1:c.*1380A=	NP_001258349.1:n.*1380A=
NM_017775.3:c.*1380A=	NP_060245.3:n.*1380A=
XM_017024801.2:c.994+2200A=	XP_016880290.2:n.994+2200A=
XM_017024802.2:c.994+2200A=	XP_016880291.2:n.994+2200A=
NM_017775.4:c.*1380A= MANE Select	NP_060245.3:n.*1380A=
NM_001271420.2:c.*1380A=	NP_001258349.1:n.*1380A=