Canonical Allele Identifier: CA10266665

Gene: TCF20

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.42210994G>A , CM000684.2:g.42210994G>A	GRCh38
NC_000022.10:g.42607000G>A , CM000684.1:g.42607000G>A	GRCh37
NC_000022.9:g.40936944G>A	NCBI36
NG_028982.3:g.137623C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001378418.1:c.4312C>T MANE Select	NP_001365347.1:p.Arg1438Cys
ENST00000677622.1:c.4312C>T MANE Select	ENSP00000503828.1:p.Arg1438Cys
NM_005650.2:c.4312C>T	NP_005641.1:p.Arg1438Cys
NM_005650.3:c.4312C>T	NP_005641.1:p.Arg1438Cys
NM_005650.4:c.4312C>T	NP_005641.1:p.Arg1438Cys
NM_181492.2:c.4312C>T	NP_852469.1:p.Arg1438Cys
NM_181492.3:c.4312C>T	NP_852469.1:p.Arg1438Cys
ENST00000335626.8:c.4312C>T	ENSP00000335561.4:p.Arg1438Cys
ENST00000359486.7:c.4312C>T	ENSP00000352463.3:p.Arg1438Cys
ENST00000359486.8:c.4312C>T	ENSP00000352463.3:p.Arg1438Cys
ENST00000683686.1:c.4312C>T	ENSP00000508272.1:p.Arg1438Cys
XM_005261722.2:c.4312C>T	XP_005261779.1:p.Arg1438Cys
XM_005261722.3:c.4312C>T	XP_005261779.1:p.Arg1438Cys
XM_006724313.2:c.4312C>T	XP_006724376.1:p.Arg1438Cys
XM_006724313.3:c.4312C>T	XP_006724376.1:p.Arg1438Cys
XM_011530353.1:c.4312C>T	XP_011528655.1:p.Arg1438Cys
XM_011530353.2:c.4312C>T	XP_011528655.1:p.Arg1438Cys
XM_011530354.1:c.4312C>T	XP_011528656.1:p.Arg1438Cys
XM_011530354.2:c.4312C>T	XP_011528656.1:p.Arg1438Cys
XM_011530355.1:c.4312C>T	XP_011528657.1:p.Arg1438Cys