Canonical Allele Identifier: CA498414372

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15903273G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999959G>C , CM000679.2:g.15999959G>C	GRCh38
NC_000017.10:g.15903273G>C , CM000679.1:g.15903273G>C	GRCh37
NC_000017.9:g.15843998G>C	NCBI36
NG_029806.1:g.5580G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.111G>C MANE Select	ENSP00000261647.5:p.Gly37=
ENST00000261647.9:c.111G>C	ENSP00000261647.5:p.Gly37=
ENST00000466729.5:c.176G>C
ENST00000470399.1:c.126G>C	ENSP00000465082.1:p.Gly42=
ENST00000475723.5:c.158G>C
ENST00000497842.6:n.136G>C
ENST00000583704.1:n.136G>C
NM_001271420.1:c.-348G>C	NP_001258349.1:n.-348G>C
NM_017775.3:c.111G>C	NP_060245.3:p.Gly37=
XM_011523950.1:c.111G>C	XP_011522252.1:p.Gly37=
XM_017024801.2:c.111G>C	XP_016880290.2:p.Gly37=
XM_017024802.2:c.111G>C	XP_016880291.2:p.Gly37=
XM_024450814.1:c.111G>C	XP_024306582.1:p.Gly37=
NM_017775.4:c.111G>C MANE Select	NP_060245.3:p.Gly37=
NM_001271420.2:c.-348G>C	NP_001258349.1:n.-348G>C