Canonical Allele Identifier: CA398379527

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15930816A>T (hg19) ; chr17:g.16027502A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027502A>T , CM000679.2:g.16027502A>T	GRCh38
NC_000017.10:g.15930816A>T , CM000679.1:g.15930816A>T	GRCh37
NC_000017.9:g.15871541A>T	NCBI36
NG_029806.1:g.33123A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1123A>T MANE Select	ENSP00000261647.5:p.Thr375Ser
ENST00000261647.9:c.1123A>T	ENSP00000261647.5:p.Thr375Ser
ENST00000465567.1:n.1517A>T
ENST00000470649.1:c.247+800A>T	ENSP00000465627.1:n.247+800A>T
ENST00000475723.5:c.1307A>T
ENST00000481107.1:n.1791A>T
ENST00000497842.6:n.1327A>T
NM_001271420.1:c.802A>T	NP_001258349.1:p.Thr268Ser
NM_017775.3:c.1123A>T	NP_060245.3:p.Thr375Ser
XM_017024801.2:c.994+800A>T	XP_016880290.2:n.994+800A>T
XM_017024802.2:c.994+800A>T	XP_016880291.2:n.994+800A>T
NM_017775.4:c.1123A>T MANE Select	NP_060245.3:p.Thr375Ser
NM_001271420.2:c.802A>T	NP_001258349.1:p.Thr268Ser