Canonical Allele Identifier: CA498414338

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15903240G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999926G>C , CM000679.2:g.15999926G>C	GRCh38
NC_000017.10:g.15903240G>C , CM000679.1:g.15903240G>C	GRCh37
NC_000017.9:g.15843965G>C	NCBI36
NG_029806.1:g.5547G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.78G>C MANE Select	ENSP00000261647.5:p.Ala26=
ENST00000261647.9:c.78G>C	ENSP00000261647.5:p.Ala26=
ENST00000466729.5:c.143G>C
ENST00000470399.1:c.93G>C	ENSP00000465082.1:p.Ala31=
ENST00000475723.5:c.125G>C
ENST00000497842.6:n.103G>C
ENST00000583704.1:n.103G>C
NM_001271420.1:c.-381G>C	NP_001258349.1:n.-381G>C
NM_017775.3:c.78G>C	NP_060245.3:p.Ala26=
XM_011523950.1:c.78G>C	XP_011522252.1:p.Ala26=
XM_017024801.2:c.78G>C	XP_016880290.2:p.Ala26=
XM_017024802.2:c.78G>C	XP_016880291.2:p.Ala26=
XM_024450814.1:c.78G>C	XP_024306582.1:p.Ala26=
NM_017775.4:c.78G>C MANE Select	NP_060245.3:p.Ala26=
NM_001271420.2:c.-381G>C	NP_001258349.1:n.-381G>C