Canonical Allele Identifier: CA398379644

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15930834T>C (hg19) ; chr17:g.16027520T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027520T>C , CM000679.2:g.16027520T>C	GRCh38
NC_000017.10:g.15930834T>C , CM000679.1:g.15930834T>C	GRCh37
NC_000017.9:g.15871559T>C	NCBI36
NG_029806.1:g.33141T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1141T>C MANE Select	ENSP00000261647.5:p.Ter381Gln
ENST00000261647.9:c.1141T>C	ENSP00000261647.5:p.Ter381Gln
ENST00000465567.1:n.1535T>C
ENST00000470649.1:c.247+818T>C	ENSP00000465627.1:n.247+818T>C
ENST00000475723.5:c.1325T>C
ENST00000481107.1:n.1809T>C
ENST00000497842.6:n.1345T>C
NM_001271420.1:c.820T>C	NP_001258349.1:p.Ter274Gln
NM_017775.3:c.1141T>C	NP_060245.3:p.Ter381Gln
XM_017024801.2:c.994+818T>C	XP_016880290.2:n.994+818T>C
XM_017024802.2:c.994+818T>C	XP_016880291.2:n.994+818T>C
NM_017775.4:c.1141T>C MANE Select	NP_060245.3:p.Ter381Gln
NM_001271420.2:c.820T>C	NP_001258349.1:p.Ter274Gln