Canonical Allele Identifier: CA942351533

Gene: TTC12

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113328424C>A , CM000673.2:g.113328424C>A	GRCh38
NC_000011.9:g.113199146C>A , CM000673.1:g.113199146C>A	GRCh37
NC_000011.8:g.112704356C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529221.6:c.445-1496C>A MANE Select	ENSP00000433757.1:n.445-1496C>A
ENST00000314756.7:c.445-1496C>A	ENSP00000315160.3:n.445-1496C>A
ENST00000393020.5:c.445-1496C>A	ENSP00000376743.1:n.445-1496C>A
ENST00000442859.5:c.445-1496C>A	ENSP00000400039.1:n.445-1496C>A
ENST00000455306.5:c.445-1496C>A	ENSP00000402004.1:n.445-1496C>A
ENST00000464224.5:c.445-1218C>A	ENSP00000437030.1:n.445-1218C>A
ENST00000483239.6:c.445-1496C>A	ENSP00000419652.2:n.445-1496C>A
ENST00000494714.5:c.445-1496C>A	ENSP00000435291.1:n.445-1496C>A
ENST00000524580.6:c.55-10350C>A	ENSP00000436677.1:n.55-10350C>A
ENST00000525965.5:c.444+2779C>A	ENSP00000435308.1:n.444+2779C>A
ENST00000527362.5:c.38-1496C>A
ENST00000529221.5:c.445-1496C>A	ENSP00000433757.1:n.445-1496C>A
ENST00000529850.5:c.444+2779C>A	ENSP00000431806.1:n.444+2779C>A
ENST00000531164.5:c.370-1496C>A	ENSP00000433916.1:n.370-1496C>A
NM_017868.3:c.445-1496C>A	NP_060338.3:n.445-1496C>A
XM_005271604.3:c.445-1496C>A	XP_005271661.1:n.445-1496C>A
XM_011542884.1:c.445-1496C>A	XP_011541186.1:n.445-1496C>A
XM_011542885.1:c.445-1496C>A	XP_011541187.1:n.445-1496C>A
XM_011542886.1:c.445-1496C>A	XP_011541188.1:n.445-1496C>A
XM_011542887.1:c.445-1496C>A	XP_011541189.1:n.445-1496C>A
XM_011542888.1:c.445-1496C>A	XP_011541190.1:n.445-1496C>A
XM_011542889.1:c.445-1496C>A	XP_011541191.1:n.445-1496C>A
XM_011542890.1:c.-173-1218C>A	XP_011541192.1:n.-173-1218C>A
XR_947856.1:n.766-1496C>A
NM_001318533.1:c.445-1496C>A	NP_001305462.1:n.445-1496C>A
NM_001352037.1:c.370-1496C>A	NP_001338966.1:n.370-1496C>A
NM_001352038.1:c.-173-1218C>A	NP_001338967.1:n.-173-1218C>A
NR_147891.1:n.550-1496C>A
XM_017017943.2:c.445-1496C>A	XP_016873432.1:n.445-1496C>A
XM_017017944.2:c.445-1496C>A	XP_016873433.1:n.445-1496C>A
XM_017017945.1:c.445-1496C>A	XP_016873434.1:n.445-1496C>A
XM_017017946.1:c.445-1496C>A	XP_016873435.1:n.445-1496C>A
XM_017017947.2:c.445-1496C>A	XP_016873436.1:n.445-1496C>A
XM_017017948.2:c.445-1496C>A	XP_016873437.1:n.445-1496C>A
XM_017017949.2:c.445-1496C>A	XP_016873438.1:n.445-1496C>A
XM_017017950.2:c.445-1496C>A	XP_016873439.1:n.445-1496C>A
XM_024448594.1:c.445-1496C>A	XP_024304362.1:n.445-1496C>A
XM_024448595.1:c.445-1496C>A	XP_024304363.1:n.445-1496C>A
XM_024448596.1:c.445-1496C>A	XP_024304364.1:n.445-1496C>A
XM_024448597.1:c.-173-1218C>A	XP_024304365.1:n.-173-1218C>A
XR_001747914.2:n.510-1496C>A
NM_001318533.2:c.445-1496C>A	NP_001305462.1:n.445-1496C>A
NM_001352037.2:c.370-1496C>A	NP_001338966.1:n.370-1496C>A
NM_001352038.2:c.-173-1218C>A	NP_001338967.1:n.-173-1218C>A
NM_017868.4:c.445-1496C>A MANE Select	NP_060338.3:n.445-1496C>A
NR_147891.2:n.496-1496C>A
NM_001378063.1:c.370-1496C>A	NP_001364992.1:n.370-1496C>A
NM_001378064.1:c.445-1496C>A	NP_001364993.1:n.445-1496C>A
NM_001378065.1:c.445-1496C>A	NP_001364994.1:n.445-1496C>A
NR_165392.1:n.1013-1218C>A
NR_165393.1:n.110-6542C>A