Canonical Allele Identifier: CA7581376

Gene: TCF12

Linked Data

• ClinVar Variation Id: 374377
• ClinVar RCV Id: RCV000415362 ; RCV001861454
• dbSNP Id: rs758543580
• ExAC: 15:57565358 C / T
• gnomAD v2: 15-57565358-C-T
• gnomAD v3: 15-57273160-C-T
• gnomAD v4: 15-57273160-C-T
• COSMIC: COSM3719418 ; COSM3719419 ; COSM3719420 ; COSM3719421
• MyVariant Identifiers: chr15:g.57565358C>T (hg19) ; chr15:g.57273160C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57273160C>T , CM000677.2:g.57273160C>T	GRCh38
NC_000015.9:g.57565358C>T , CM000677.1:g.57565358C>T	GRCh37
NC_000015.8:g.55352650C>T	NCBI36
NG_033851.1:g.359526C>T
NG_033851.2:g.360071C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333725.10:c.1876C>T MANE Select	ENSP00000331057.6:p.Arg626Ter
ENST00000267811.9:c.1804C>T	ENSP00000267811.5:p.Arg602Ter
ENST00000333725.9:c.1876C>T	ENSP00000331057.5:p.Arg626Ter
ENST00000343827.7:c.1294C>T	ENSP00000342459.3:p.Arg432Ter
ENST00000438423.6:c.1876C>T	ENSP00000388940.2:p.Arg626Ter
ENST00000537840.5:c.1096C>T	ENSP00000444696.1:p.Arg366Ter
ENST00000543579.5:c.1366C>T	ENSP00000440017.1:p.Arg456Ter
ENST00000557843.5:c.1804C>T	ENSP00000453737.1:p.Arg602Ter
ENST00000559609.5:c.1864C>T	ENSP00000453876.1:p.Arg622Ter
ENST00000559703.1:c.775C>T	ENSP00000454102.1:p.Arg259Ter
ENST00000559710.5:c.706C>T	ENSP00000453264.1:p.Arg236Ter
ENST00000560190.5:n.533C>T
ENST00000561420.5:n.799C>T
ENST00000561449.1:n.910C>T
NM_001306219.1:c.1366C>T	NP_001293148.1:p.Arg456Ter
NM_001306220.1:c.1096C>T	NP_001293149.1:p.Arg366Ter
NM_003205.3:c.1804C>T	NP_003196.1:p.Arg602Ter
NM_207036.1:c.1876C>T	NP_996919.1:p.Arg626Ter
NM_207037.1:c.1876C>T	NP_996920.1:p.Arg626Ter
NM_207038.1:c.1804C>T	NP_996921.1:p.Arg602Ter
NM_207040.1:c.1294C>T	NP_996923.1:p.Arg432Ter
XM_005254613.3:c.1702C>T	XP_005254670.1:p.Arg568Ter
XM_011521959.1:c.1912C>T	XP_011520261.1:p.Arg638Ter
XM_011521960.1:c.1912C>T	XP_011520262.1:p.Arg638Ter
XM_011521961.1:c.1909C>T	XP_011520263.1:p.Arg637Ter
XM_011521962.1:c.1840C>T	XP_011520264.1:p.Arg614Ter
XM_011521963.1:c.1837C>T	XP_011520265.1:p.Arg613Ter
XM_011521965.1:c.1228C>T	XP_011520267.1:p.Arg410Ter
XM_011521966.1:c.1168C>T	XP_011520268.1:p.Arg390Ter
XM_011521967.1:c.1156C>T	XP_011520269.1:p.Arg386Ter
XM_011521969.1:c.1291C>T	XP_011520271.1:p.Arg431Ter
NM_001306219.2:c.1366C>T	NP_001293148.1:p.Arg456Ter
NM_001306220.2:c.1096C>T	NP_001293149.1:p.Arg366Ter
NM_001322151.1:c.1876C>T	NP_001309080.1:p.Arg626Ter
NM_001322152.1:c.1873C>T	NP_001309081.1:p.Arg625Ter
NM_001322154.1:c.1219C>T	NP_001309083.1:p.Arg407Ter
NM_001322156.1:c.1702C>T	NP_001309085.1:p.Arg568Ter
NM_001322157.1:c.1804C>T	NP_001309086.1:p.Arg602Ter
NM_001322158.1:c.1630C>T	NP_001309087.1:p.Arg544Ter
NM_001322159.1:c.1876C>T	NP_001309088.1:p.Arg626Ter
NM_001322161.1:c.1873C>T	NP_001309090.1:p.Arg625Ter
NM_001322162.1:c.1876C>T	NP_001309091.1:p.Arg626Ter
NM_001322164.1:c.1840C>T	NP_001309093.1:p.Arg614Ter
NM_001322165.1:c.1804C>T	NP_001309094.1:p.Arg602Ter
XM_011521959.3:c.1912C>T	XP_011520261.1:p.Arg638Ter
XM_011521960.3:c.1912C>T	XP_011520262.1:p.Arg638Ter
XM_011521961.3:c.1909C>T	XP_011520263.1:p.Arg637Ter
XM_011521962.3:c.1840C>T	XP_011520264.1:p.Arg614Ter
XM_011521963.3:c.1837C>T	XP_011520265.1:p.Arg613Ter
XM_011521965.2:c.1228C>T	XP_011520267.1:p.Arg410Ter
XM_011521966.2:c.1168C>T	XP_011520268.1:p.Arg390Ter
XM_011521967.2:c.1156C>T	XP_011520269.1:p.Arg386Ter
XM_017022520.2:c.1801C>T	XP_016878009.1:p.Arg601Ter
NM_001306219.3:c.1366C>T	NP_001293148.1:p.Arg456Ter
NM_001306220.3:c.1096C>T	NP_001293149.1:p.Arg366Ter
NM_001322152.2:c.1873C>T	NP_001309081.1:p.Arg625Ter
NM_001322154.2:c.1219C>T	NP_001309083.1:p.Arg407Ter
NM_001322156.2:c.1702C>T	NP_001309085.1:p.Arg568Ter
NM_001322157.2:c.1804C>T	NP_001309086.1:p.Arg602Ter
NM_001322158.2:c.1630C>T	NP_001309087.1:p.Arg544Ter
NM_001322159.2:c.1876C>T	NP_001309088.1:p.Arg626Ter
NM_001322161.2:c.1873C>T	NP_001309090.1:p.Arg625Ter
NM_001322162.2:c.1876C>T	NP_001309091.1:p.Arg626Ter
NM_001322164.2:c.1840C>T	NP_001309093.1:p.Arg614Ter
NM_001322165.2:c.1804C>T	NP_001309094.1:p.Arg602Ter
NM_003205.4:c.1804C>T	NP_003196.1:p.Arg602Ter
NM_207036.2:c.1876C>T	NP_996919.1:p.Arg626Ter
NM_207037.2:c.1876C>T MANE Select	NP_996920.1:p.Arg626Ter
NM_207038.2:c.1804C>T	NP_996921.1:p.Arg602Ter
NM_207040.2:c.1294C>T	NP_996923.1:p.Arg432Ter
NM_001322151.2:c.1876C>T	NP_001309080.1:p.Arg626Ter
NM_001322157.3:c.1804C>T	NP_001309086.1:p.Arg602Ter
NM_001322159.3:c.1876C>T	NP_001309088.1:p.Arg626Ter