Canonical Allele Identifier: CA2628635630
Gene: TCF12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.57262028T>A , CM000677.2:g.57262028T>A GRCh38
NC_000015.9:g.57554226T>A , CM000677.1:g.57554226T>A GRCh37
NC_000015.8:g.55341518T>A NCBI36
NG_033851.1:g.348394T>A
NG_033851.2:g.348939T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000333725.10:c.1468-66T>A MANE Select ENSP00000331057.6:n.1468-66T>A
ENST00000267811.9:c.1396-66T>A ENSP00000267811.5:n.1396-66T>A
ENST00000333725.9:c.1468-66T>A ENSP00000331057.5:n.1468-66T>A
ENST00000343827.7:c.886-66T>A ENSP00000342459.3:n.886-66T>A
ENST00000438423.6:c.1468-66T>A ENSP00000388940.2:n.1468-66T>A
ENST00000537840.5:c.688-66T>A ENSP00000444696.1:n.688-66T>A
ENST00000543579.5:c.958-66T>A ENSP00000440017.1:n.958-66T>A
ENST00000557843.5:c.1396-66T>A ENSP00000453737.1:n.1396-66T>A
ENST00000558210.5:n.535-66T>A
ENST00000559609.5:c.1456-66T>A ENSP00000453876.1:n.1456-66T>A
ENST00000559703.1:c.370-66T>A ENSP00000454102.1:n.370-66T>A
ENST00000559710.5:c.298-66T>A ENSP00000453264.1:n.298-66T>A
ENST00000560190.5:n.403-11002T>A
ENST00000560506.5:n.348-66T>A
ENST00000561420.5:n.394-66T>A
ENST00000561449.1:n.502-66T>A
NM_001306219.1:c.958-66T>A NP_001293148.1:n.958-66T>A
NM_001306220.1:c.688-66T>A NP_001293149.1:n.688-66T>A
NM_003205.3:c.1396-66T>A NP_003196.1:n.1396-66T>A
NM_207036.1:c.1468-66T>A NP_996919.1:n.1468-66T>A
NM_207037.1:c.1468-66T>A NP_996920.1:n.1468-66T>A
NM_207038.1:c.1396-66T>A NP_996921.1:n.1396-66T>A
NM_207040.1:c.886-66T>A NP_996923.1:n.886-66T>A
XM_005254613.3:c.1294-66T>A XP_005254670.1:n.1294-66T>A
XM_011521959.1:c.1504-66T>A XP_011520261.1:n.1504-66T>A
XM_011521960.1:c.1504-66T>A XP_011520262.1:n.1504-66T>A
XM_011521961.1:c.1504-66T>A XP_011520263.1:n.1504-66T>A
XM_011521962.1:c.1432-66T>A XP_011520264.1:n.1432-66T>A
XM_011521963.1:c.1432-66T>A XP_011520265.1:n.1432-66T>A
XM_011521965.1:c.820-66T>A XP_011520267.1:n.820-66T>A
XM_011521966.1:c.760-66T>A XP_011520268.1:n.760-66T>A
XM_011521967.1:c.748-66T>A XP_011520269.1:n.748-66T>A
XM_011521969.1:c.886-66T>A XP_011520271.1:n.886-66T>A
NM_001306219.2:c.958-66T>A NP_001293148.1:n.958-66T>A
NM_001306220.2:c.688-66T>A NP_001293149.1:n.688-66T>A
NM_001322151.1:c.1468-66T>A NP_001309080.1:n.1468-66T>A
NM_001322152.1:c.1468-66T>A NP_001309081.1:n.1468-66T>A
NM_001322154.1:c.811-66T>A NP_001309083.1:n.811-66T>A
NM_001322156.1:c.1294-66T>A NP_001309085.1:n.1294-66T>A
NM_001322157.1:c.1396-66T>A NP_001309086.1:n.1396-66T>A
NM_001322158.1:c.1222-66T>A NP_001309087.1:n.1222-66T>A
NM_001322159.1:c.1468-66T>A NP_001309088.1:n.1468-66T>A
NM_001322161.1:c.1465-66T>A NP_001309090.1:n.1465-66T>A
NM_001322162.1:c.1468-66T>A NP_001309091.1:n.1468-66T>A
NM_001322164.1:c.1432-66T>A NP_001309093.1:n.1432-66T>A
NM_001322165.1:c.1396-66T>A NP_001309094.1:n.1396-66T>A
XM_011521959.3:c.1504-66T>A XP_011520261.1:n.1504-66T>A
XM_011521960.3:c.1504-66T>A XP_011520262.1:n.1504-66T>A
XM_011521961.3:c.1504-66T>A XP_011520263.1:n.1504-66T>A
XM_011521962.3:c.1432-66T>A XP_011520264.1:n.1432-66T>A
XM_011521963.3:c.1432-66T>A XP_011520265.1:n.1432-66T>A
XM_011521965.2:c.820-66T>A XP_011520267.1:n.820-66T>A
XM_011521966.2:c.760-66T>A XP_011520268.1:n.760-66T>A
XM_011521967.2:c.748-66T>A XP_011520269.1:n.748-66T>A
XM_017022520.2:c.1396-66T>A XP_016878009.1:n.1396-66T>A
NM_001306219.3:c.958-66T>A NP_001293148.1:n.958-66T>A
NM_001306220.3:c.688-66T>A NP_001293149.1:n.688-66T>A
NM_001322152.2:c.1468-66T>A NP_001309081.1:n.1468-66T>A
NM_001322154.2:c.811-66T>A NP_001309083.1:n.811-66T>A
NM_001322156.2:c.1294-66T>A NP_001309085.1:n.1294-66T>A
NM_001322157.2:c.1396-66T>A NP_001309086.1:n.1396-66T>A
NM_001322158.2:c.1222-66T>A NP_001309087.1:n.1222-66T>A
NM_001322159.2:c.1468-66T>A NP_001309088.1:n.1468-66T>A
NM_001322161.2:c.1465-66T>A NP_001309090.1:n.1465-66T>A
NM_001322162.2:c.1468-66T>A NP_001309091.1:n.1468-66T>A
NM_001322164.2:c.1432-66T>A NP_001309093.1:n.1432-66T>A
NM_001322165.2:c.1396-66T>A NP_001309094.1:n.1396-66T>A
NM_003205.4:c.1396-66T>A NP_003196.1:n.1396-66T>A
NM_207036.2:c.1468-66T>A NP_996919.1:n.1468-66T>A
NM_207037.2:c.1468-66T>A MANE Select NP_996920.1:n.1468-66T>A
NM_207038.2:c.1396-66T>A NP_996921.1:n.1396-66T>A
NM_207040.2:c.886-66T>A NP_996923.1:n.886-66T>A
NM_001322151.2:c.1468-66T>A NP_001309080.1:n.1468-66T>A
NM_001322157.3:c.1396-66T>A NP_001309086.1:n.1396-66T>A
NM_001322159.3:c.1468-66T>A NP_001309088.1:n.1468-66T>A