Canonical Allele Identifier: CA2830558160

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027566A>G , CM000679.2:g.16027566A>G	GRCh38
NC_000017.10:g.15930880A>G , CM000679.1:g.15930880A>G	GRCh37
NC_000017.9:g.15871605A>G	NCBI36
NG_029806.1:g.33187A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*44A>G MANE Select	ENSP00000261647.5:n.*44A>G
ENST00000261647.9:c.*44A>G	ENSP00000261647.5:n.*44A>G
ENST00000465567.1:n.1581A>G
ENST00000470649.1:c.247+864A>G	ENSP00000465627.1:n.247+864A>G
ENST00000475723.5:c.1371A>G
ENST00000481107.1:n.1855A>G
NM_001271420.1:c.*44A>G	NP_001258349.1:n.*44A>G
NM_017775.3:c.*44A>G	NP_060245.3:n.*44A>G
XM_017024801.2:c.994+864A>G	XP_016880290.2:n.994+864A>G
XM_017024802.2:c.994+864A>G	XP_016880291.2:n.994+864A>G
NM_017775.4:c.*44A>G MANE Select	NP_060245.3:n.*44A>G
NM_001271420.2:c.*44A>G	NP_001258349.1:n.*44A>G