Canonical Allele Identifier: CA392592492

Gene: TCF12

Linked Data

• MyVariant Identifiers: chr15:g.57524926C>A (hg19) ; chr15:g.57232728C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57232728C>A , CM000677.2:g.57232728C>A	GRCh38
NC_000015.9:g.57524926C>A , CM000677.1:g.57524926C>A	GRCh37
NC_000015.8:g.55312218C>A	NCBI36
NG_033851.1:g.319094C>A
NG_033851.2:g.319639C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333725.10:c.842C>A MANE Select	ENSP00000331057.6:p.Ser281Ter
ENST00000267811.9:c.842C>A	ENSP00000267811.5:p.Ser281Ter
ENST00000333725.9:c.842C>A	ENSP00000331057.5:p.Ser281Ter
ENST00000343827.7:c.332C>A	ENSP00000342459.3:p.Ser111Ter
ENST00000438423.6:c.842C>A	ENSP00000388940.2:p.Ser281Ter
ENST00000537840.5:c.134C>A	ENSP00000444696.1:p.Ser45Ter
ENST00000543579.5:c.332C>A	ENSP00000440017.1:p.Ser111Ter
ENST00000557843.5:c.842C>A	ENSP00000453737.1:p.Ser281Ter
ENST00000559609.5:c.830C>A	ENSP00000453876.1:p.Ser277Ter
ENST00000560190.5:n.403-40302C>A
ENST00000560764.5:n.677C>A
ENST00000561235.5:n.581C>A
ENST00000561346.5:n.577C>A
NM_001306219.1:c.332C>A	NP_001293148.1:p.Ser111Ter
NM_001306220.1:c.134C>A	NP_001293149.1:p.Ser45Ter
NM_003205.3:c.842C>A	NP_003196.1:p.Ser281Ter
NM_207036.1:c.842C>A	NP_996919.1:p.Ser281Ter
NM_207037.1:c.842C>A	NP_996920.1:p.Ser281Ter
NM_207038.1:c.842C>A	NP_996921.1:p.Ser281Ter
NM_207040.1:c.332C>A	NP_996923.1:p.Ser111Ter
XM_005254613.3:c.668C>A	XP_005254670.1:p.Ser223Ter
XM_011521959.1:c.878C>A	XP_011520261.1:p.Ser293Ter
XM_011521960.1:c.878C>A	XP_011520262.1:p.Ser293Ter
XM_011521961.1:c.878C>A	XP_011520263.1:p.Ser293Ter
XM_011521962.1:c.878C>A	XP_011520264.1:p.Ser293Ter
XM_011521963.1:c.878C>A	XP_011520265.1:p.Ser293Ter
XM_011521965.1:c.194C>A	XP_011520267.1:p.Ser65Ter
XM_011521966.1:c.134C>A	XP_011520268.1:p.Ser45Ter
XM_011521967.1:c.194C>A	XP_011520269.1:p.Ser65Ter
XM_011521969.1:c.332C>A	XP_011520271.1:p.Ser111Ter
NM_001306219.2:c.332C>A	NP_001293148.1:p.Ser111Ter
NM_001306220.2:c.134C>A	NP_001293149.1:p.Ser45Ter
NM_001322151.1:c.842C>A	NP_001309080.1:p.Ser281Ter
NM_001322152.1:c.842C>A	NP_001309081.1:p.Ser281Ter
NM_001322154.1:c.185C>A	NP_001309083.1:p.Ser62Ter
NM_001322156.1:c.668C>A	NP_001309085.1:p.Ser223Ter
NM_001322157.1:c.842C>A	NP_001309086.1:p.Ser281Ter
NM_001322158.1:c.668C>A	NP_001309087.1:p.Ser223Ter
NM_001322159.1:c.842C>A	NP_001309088.1:p.Ser281Ter
NM_001322161.1:c.842C>A	NP_001309090.1:p.Ser281Ter
NM_001322162.1:c.842C>A	NP_001309091.1:p.Ser281Ter
NM_001322164.1:c.878C>A	NP_001309093.1:p.Ser293Ter
NM_001322165.1:c.842C>A	NP_001309094.1:p.Ser281Ter
XM_011521959.3:c.878C>A	XP_011520261.1:p.Ser293Ter
XM_011521960.3:c.878C>A	XP_011520262.1:p.Ser293Ter
XM_011521961.3:c.878C>A	XP_011520263.1:p.Ser293Ter
XM_011521962.3:c.878C>A	XP_011520264.1:p.Ser293Ter
XM_011521963.3:c.878C>A	XP_011520265.1:p.Ser293Ter
XM_011521965.2:c.194C>A	XP_011520267.1:p.Ser65Ter
XM_011521966.2:c.134C>A	XP_011520268.1:p.Ser45Ter
XM_011521967.2:c.194C>A	XP_011520269.1:p.Ser65Ter
XM_017022520.2:c.842C>A	XP_016878009.1:p.Ser281Ter
NM_001306219.3:c.332C>A	NP_001293148.1:p.Ser111Ter
NM_001306220.3:c.134C>A	NP_001293149.1:p.Ser45Ter
NM_001322152.2:c.842C>A	NP_001309081.1:p.Ser281Ter
NM_001322154.2:c.185C>A	NP_001309083.1:p.Ser62Ter
NM_001322156.2:c.668C>A	NP_001309085.1:p.Ser223Ter
NM_001322157.2:c.842C>A	NP_001309086.1:p.Ser281Ter
NM_001322158.2:c.668C>A	NP_001309087.1:p.Ser223Ter
NM_001322159.2:c.842C>A	NP_001309088.1:p.Ser281Ter
NM_001322161.2:c.842C>A	NP_001309090.1:p.Ser281Ter
NM_001322162.2:c.842C>A	NP_001309091.1:p.Ser281Ter
NM_001322164.2:c.878C>A	NP_001309093.1:p.Ser293Ter
NM_001322165.2:c.842C>A	NP_001309094.1:p.Ser281Ter
NM_003205.4:c.842C>A	NP_003196.1:p.Ser281Ter
NM_207036.2:c.842C>A	NP_996919.1:p.Ser281Ter
NM_207037.2:c.842C>A MANE Select	NP_996920.1:p.Ser281Ter
NM_207038.2:c.842C>A	NP_996921.1:p.Ser281Ter
NM_207040.2:c.332C>A	NP_996923.1:p.Ser111Ter
NM_001322151.2:c.842C>A	NP_001309080.1:p.Ser281Ter
NM_001322157.3:c.842C>A	NP_001309086.1:p.Ser281Ter
NM_001322159.3:c.842C>A	NP_001309088.1:p.Ser281Ter