Canonical Allele Identifier: CA2249871778

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028763A= , CM000679.2:g.16028763A=	GRCh38
NC_000017.10:g.15932077A= , CM000679.1:g.15932077A=	GRCh37
NC_000017.9:g.15872802A=	NCBI36
NG_029806.1:g.34384A=
NG_047111.1:g.192984T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*1241A= MANE Select	ENSP00000261647.5:n.*1241A=
ENST00000261647.9:c.*1241A=	ENSP00000261647.5:n.*1241A=
ENST00000465567.1:n.2778A=
ENST00000470649.1:c.247+2061A=	ENSP00000465627.1:n.247+2061A=
ENST00000475723.5:c.2568A=
ENST00000481107.1:n.3052A=
NM_001271420.1:c.*1241A=	NP_001258349.1:n.*1241A=
NM_017775.3:c.*1241A=	NP_060245.3:n.*1241A=
XM_017024801.2:c.994+2061A=	XP_016880290.2:n.994+2061A=
XM_017024802.2:c.994+2061A=	XP_016880291.2:n.994+2061A=
NM_017775.4:c.*1241A= MANE Select	NP_060245.3:n.*1241A=
NM_001271420.2:c.*1241A=	NP_001258349.1:n.*1241A=