Canonical Allele Identifier: CA714146726

Gene: TCF12

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.56997172C>G , CM000677.2:g.56997172C>G	GRCh38
NC_000015.9:g.57289370C>G , CM000677.1:g.57289370C>G	GRCh37
NC_000015.8:g.55076662C>G	NCBI36
NG_033851.1:g.83538C>G
NG_033851.2:g.84083C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_207037.2:c.149-66578C>G MANE Select	NP_996920.1:n.149-66578C>G
ENST00000333725.10:c.149-66578C>G MANE Select	ENSP00000331057.6:n.149-66578C>G
NM_001322151.1:c.149-66578C>G	NP_001309080.1:n.149-66578C>G
NM_001322151.2:c.149-66578C>G	NP_001309080.1:n.149-66578C>G
NM_001322152.1:c.149-66578C>G	NP_001309081.1:n.149-66578C>G
NM_001322152.2:c.149-66578C>G	NP_001309081.1:n.149-66578C>G
NM_001322154.1:c.-504-66578C>G	NP_001309083.1:n.-504-66578C>G
NM_001322154.2:c.-504-66578C>G	NP_001309083.1:n.-504-66578C>G
NM_001322156.1:c.-88-66578C>G	NP_001309085.1:n.-88-66578C>G
NM_001322156.2:c.-88-66578C>G	NP_001309085.1:n.-88-66578C>G
NM_001322157.1:c.149-66578C>G	NP_001309086.1:n.149-66578C>G
NM_001322157.2:c.149-66578C>G	NP_001309086.1:n.149-66578C>G
NM_001322157.3:c.149-66578C>G	NP_001309086.1:n.149-66578C>G
NM_001322158.1:c.-88-66578C>G	NP_001309087.1:n.-88-66578C>G
NM_001322158.2:c.-88-66578C>G	NP_001309087.1:n.-88-66578C>G
NM_001322159.1:c.149-66578C>G	NP_001309088.1:n.149-66578C>G
NM_001322159.2:c.149-66578C>G	NP_001309088.1:n.149-66578C>G
NM_001322159.3:c.149-66578C>G	NP_001309088.1:n.149-66578C>G
NM_001322161.1:c.149-66578C>G	NP_001309090.1:n.149-66578C>G
NM_001322161.2:c.149-66578C>G	NP_001309090.1:n.149-66578C>G
NM_001322162.1:c.149-66578C>G	NP_001309091.1:n.149-66578C>G
NM_001322162.2:c.149-66578C>G	NP_001309091.1:n.149-66578C>G
NM_001322164.1:c.149-4177C>G	NP_001309093.1:n.149-4177C>G
NM_001322164.2:c.149-4177C>G	NP_001309093.1:n.149-4177C>G
NM_001322165.1:c.149-66578C>G	NP_001309094.1:n.149-66578C>G
NM_001322165.2:c.149-66578C>G	NP_001309094.1:n.149-66578C>G
NM_003205.3:c.149-66578C>G	NP_003196.1:n.149-66578C>G
NM_003205.4:c.149-66578C>G	NP_003196.1:n.149-66578C>G
NM_207036.1:c.149-66578C>G	NP_996919.1:n.149-66578C>G
NM_207036.2:c.149-66578C>G	NP_996919.1:n.149-66578C>G
NM_207037.1:c.149-66578C>G	NP_996920.1:n.149-66578C>G
NM_207038.1:c.149-66578C>G	NP_996921.1:n.149-66578C>G
NM_207038.2:c.149-66578C>G	NP_996921.1:n.149-66578C>G
ENST00000267811.9:c.149-66578C>G	ENSP00000267811.5:n.149-66578C>G
ENST00000333725.9:c.149-66578C>G	ENSP00000331057.5:n.149-66578C>G
ENST00000438423.6:c.149-66578C>G	ENSP00000388940.2:n.149-66578C>G
ENST00000557843.5:c.149-66578C>G	ENSP00000453737.1:n.149-66578C>G
ENST00000557947.5:c.149-66578C>G	ENSP00000454109.1:n.149-66578C>G
ENST00000558908.5:n.403-4177C>G
ENST00000559609.5:c.149-75481C>G	ENSP00000453876.1:n.149-75481C>G
ENST00000560190.5:n.402+76074C>G
ENST00000561152.1:c.148+76074C>G	ENSP00000453653.1:n.148+76074C>G
XM_005254613.3:c.-88-66578C>G	XP_005254670.1:n.-88-66578C>G
XM_011521959.1:c.149-4177C>G	XP_011520261.1:n.149-4177C>G
XM_011521959.3:c.149-4177C>G	XP_011520261.1:n.149-4177C>G
XM_011521960.1:c.149-4177C>G	XP_011520262.1:n.149-4177C>G
XM_011521960.3:c.149-4177C>G	XP_011520262.1:n.149-4177C>G
XM_011521961.1:c.149-4177C>G	XP_011520263.1:n.149-4177C>G
XM_011521961.3:c.149-4177C>G	XP_011520263.1:n.149-4177C>G
XM_011521962.1:c.149-4177C>G	XP_011520264.1:n.149-4177C>G
XM_011521962.3:c.149-4177C>G	XP_011520264.1:n.149-4177C>G
XM_011521963.1:c.149-4177C>G	XP_011520265.1:n.149-4177C>G
XM_011521963.3:c.149-4177C>G	XP_011520265.1:n.149-4177C>G
XM_011521965.1:c.-360-66578C>G	XP_011520267.1:n.-360-66578C>G
XM_011521965.2:c.-360-66578C>G	XP_011520267.1:n.-360-66578C>G
XM_011521967.1:c.-360-66578C>G	XP_011520269.1:n.-360-66578C>G
XM_011521967.2:c.-360-66578C>G	XP_011520269.1:n.-360-66578C>G
XM_017022520.2:c.149-66578C>G	XP_016878009.1:n.149-66578C>G