Canonical Allele Identifier: CA10581401

Gene: TCF12

Linked Data

• ClinVar Variation Id: 235692
• ClinVar RCV Id: RCV000224406 ; RCV001283796
• dbSNP Id: rs878853094
• gnomAD v4: 15-57234112-G-A
• MyVariant Identifiers: chr15:g.57526310G>A (hg19) ; chr15:g.57234112G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57234112G>A , CM000677.2:g.57234112G>A	GRCh38
NC_000015.9:g.57526310G>A , CM000677.1:g.57526310G>A	GRCh37
NC_000015.8:g.55313602G>A	NCBI36
NG_033851.1:g.320478G>A
NG_033851.2:g.321023G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333725.10:c.1035+5G>A MANE Select	ENSP00000331057.6:n.1035+5G>A
ENST00000267811.9:c.1035+5G>A	ENSP00000267811.5:n.1035+5G>A
ENST00000333725.9:c.1035+5G>A	ENSP00000331057.5:n.1035+5G>A
ENST00000343827.7:c.525+5G>A	ENSP00000342459.3:n.525+5G>A
ENST00000438423.6:c.1035+5G>A	ENSP00000388940.2:n.1035+5G>A
ENST00000537840.5:c.327+5G>A	ENSP00000444696.1:n.327+5G>A
ENST00000543579.5:c.525+5G>A	ENSP00000440017.1:n.525+5G>A
ENST00000557843.5:c.1035+5G>A	ENSP00000453737.1:n.1035+5G>A
ENST00000559609.5:c.1023+5G>A	ENSP00000453876.1:n.1023+5G>A
ENST00000560190.5:n.403-38918G>A
ENST00000560764.5:n.870+5G>A
ENST00000561235.5:n.774+5G>A
ENST00000561346.5:n.770+5G>A
NM_001306219.1:c.525+5G>A	NP_001293148.1:n.525+5G>A
NM_001306220.1:c.327+5G>A	NP_001293149.1:n.327+5G>A
NM_003205.3:c.1035+5G>A	NP_003196.1:n.1035+5G>A
NM_207036.1:c.1035+5G>A	NP_996919.1:n.1035+5G>A
NM_207037.1:c.1035+5G>A	NP_996920.1:n.1035+5G>A
NM_207038.1:c.1035+5G>A	NP_996921.1:n.1035+5G>A
NM_207040.1:c.525+5G>A	NP_996923.1:n.525+5G>A
XM_005254613.3:c.861+5G>A	XP_005254670.1:n.861+5G>A
XM_011521959.1:c.1071+5G>A	XP_011520261.1:n.1071+5G>A
XM_011521960.1:c.1071+5G>A	XP_011520262.1:n.1071+5G>A
XM_011521961.1:c.1071+5G>A	XP_011520263.1:n.1071+5G>A
XM_011521962.1:c.1071+5G>A	XP_011520264.1:n.1071+5G>A
XM_011521963.1:c.1071+5G>A	XP_011520265.1:n.1071+5G>A
XM_011521965.1:c.387+5G>A	XP_011520267.1:n.387+5G>A
XM_011521966.1:c.327+5G>A	XP_011520268.1:n.327+5G>A
XM_011521967.1:c.387+5G>A	XP_011520269.1:n.387+5G>A
XM_011521969.1:c.525+5G>A	XP_011520271.1:n.525+5G>A
NM_001306219.2:c.525+5G>A	NP_001293148.1:n.525+5G>A
NM_001306220.2:c.327+5G>A	NP_001293149.1:n.327+5G>A
NM_001322151.1:c.1035+5G>A	NP_001309080.1:n.1035+5G>A
NM_001322152.1:c.1035+5G>A	NP_001309081.1:n.1035+5G>A
NM_001322154.1:c.378+5G>A	NP_001309083.1:n.378+5G>A
NM_001322156.1:c.861+5G>A	NP_001309085.1:n.861+5G>A
NM_001322157.1:c.1035+5G>A	NP_001309086.1:n.1035+5G>A
NM_001322158.1:c.861+5G>A	NP_001309087.1:n.861+5G>A
NM_001322159.1:c.1035+5G>A	NP_001309088.1:n.1035+5G>A
NM_001322161.1:c.1035+5G>A	NP_001309090.1:n.1035+5G>A
NM_001322162.1:c.1035+5G>A	NP_001309091.1:n.1035+5G>A
NM_001322164.1:c.1071+5G>A	NP_001309093.1:n.1071+5G>A
NM_001322165.1:c.1035+5G>A	NP_001309094.1:n.1035+5G>A
XM_011521959.3:c.1071+5G>A	XP_011520261.1:n.1071+5G>A
XM_011521960.3:c.1071+5G>A	XP_011520262.1:n.1071+5G>A
XM_011521961.3:c.1071+5G>A	XP_011520263.1:n.1071+5G>A
XM_011521962.3:c.1071+5G>A	XP_011520264.1:n.1071+5G>A
XM_011521963.3:c.1071+5G>A	XP_011520265.1:n.1071+5G>A
XM_011521965.2:c.387+5G>A	XP_011520267.1:n.387+5G>A
XM_011521966.2:c.327+5G>A	XP_011520268.1:n.327+5G>A
XM_011521967.2:c.387+5G>A	XP_011520269.1:n.387+5G>A
XM_017022520.2:c.1035+5G>A	XP_016878009.1:n.1035+5G>A
NM_001306219.3:c.525+5G>A	NP_001293148.1:n.525+5G>A
NM_001306220.3:c.327+5G>A	NP_001293149.1:n.327+5G>A
NM_001322152.2:c.1035+5G>A	NP_001309081.1:n.1035+5G>A
NM_001322154.2:c.378+5G>A	NP_001309083.1:n.378+5G>A
NM_001322156.2:c.861+5G>A	NP_001309085.1:n.861+5G>A
NM_001322157.2:c.1035+5G>A	NP_001309086.1:n.1035+5G>A
NM_001322158.2:c.861+5G>A	NP_001309087.1:n.861+5G>A
NM_001322159.2:c.1035+5G>A	NP_001309088.1:n.1035+5G>A
NM_001322161.2:c.1035+5G>A	NP_001309090.1:n.1035+5G>A
NM_001322162.2:c.1035+5G>A	NP_001309091.1:n.1035+5G>A
NM_001322164.2:c.1071+5G>A	NP_001309093.1:n.1071+5G>A
NM_001322165.2:c.1035+5G>A	NP_001309094.1:n.1035+5G>A
NM_003205.4:c.1035+5G>A	NP_003196.1:n.1035+5G>A
NM_207036.2:c.1035+5G>A	NP_996919.1:n.1035+5G>A
NM_207037.2:c.1035+5G>A MANE Select	NP_996920.1:n.1035+5G>A
NM_207038.2:c.1035+5G>A	NP_996921.1:n.1035+5G>A
NM_207040.2:c.525+5G>A	NP_996923.1:n.525+5G>A
NM_001322151.2:c.1035+5G>A	NP_001309080.1:n.1035+5G>A
NM_001322157.3:c.1035+5G>A	NP_001309086.1:n.1035+5G>A
NM_001322159.3:c.1035+5G>A	NP_001309088.1:n.1035+5G>A