Canonical Allele Identifier: CA2581296541

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028231T>G , CM000679.2:g.16028231T>G	GRCh38
NC_000017.10:g.15931545T>G , CM000679.1:g.15931545T>G	GRCh37
NC_000017.9:g.15872270T>G	NCBI36
NG_029806.1:g.33852T>G
NG_047111.1:g.193516A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*709T>G MANE Select	ENSP00000261647.5:n.*709T>G
ENST00000261647.9:c.*709T>G	ENSP00000261647.5:n.*709T>G
ENST00000465567.1:n.2246T>G
ENST00000470649.1:c.247+1529T>G	ENSP00000465627.1:n.247+1529T>G
ENST00000475723.5:c.2036T>G
ENST00000481107.1:n.2520T>G
NM_001271420.1:c.*709T>G	NP_001258349.1:n.*709T>G
NM_017775.3:c.*709T>G	NP_060245.3:n.*709T>G
XM_017024801.2:c.994+1529T>G	XP_016880290.2:n.994+1529T>G
XM_017024802.2:c.994+1529T>G	XP_016880291.2:n.994+1529T>G
NM_017775.4:c.*709T>G MANE Select	NP_060245.3:n.*709T>G
NM_001271420.2:c.*709T>G	NP_001258349.1:n.*709T>G