Canonical Allele Identifier: CA2249872538

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028888A= , CM000679.2:g.16028888A=	GRCh38
NC_000017.10:g.15932202A= , CM000679.1:g.15932202A=	GRCh37
NC_000017.9:g.15872927A=	NCBI36
NG_029806.1:g.34509A=
NG_047111.1:g.192859T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1366A= MANE Select	ENSP00000261647.5:n.*1366A=
ENST00000261647.9:c.*1366A=	ENSP00000261647.5:n.*1366A=
ENST00000470649.1:c.247+2186A=	ENSP00000465627.1:n.247+2186A=
NM_001271420.1:c.*1366A=	NP_001258349.1:n.*1366A=
NM_017775.3:c.*1366A=	NP_060245.3:n.*1366A=
XM_017024801.2:c.994+2186A=	XP_016880290.2:n.994+2186A=
XM_017024802.2:c.994+2186A=	XP_016880291.2:n.994+2186A=
NM_017775.4:c.*1366A= MANE Select	NP_060245.3:n.*1366A=
NM_001271420.2:c.*1366A=	NP_001258349.1:n.*1366A=