Canonical Allele Identifier: CA915946176

Gene: NR2F2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.96337406_96337412del , CM000677.2:g.96337406_96337412del	GRCh38
NC_000015.9:g.96880635_96880641del , CM000677.1:g.96880635_96880641del	GRCh37
NC_000015.8:g.94681639_94681645del	NCBI36
NG_016753.1:g.16479_16485del

Transcript Alleles

HGVS	Amino-acid Change
NM_021005.4:c.1029_1035del MANE Select	NP_066285.1:p.Cys343TrpfsTer?
ENST00000394166.8:c.1029_1035del MANE Select	ENSP00000377721.3:p.Cys343TrpfsTer?
NM_001145155.1:c.630_636del	NP_001138627.1:p.Cys210TrpfsTer?
NM_001145155.2:c.630_636del	NP_001138627.1:p.Cys210TrpfsTer?
NM_001145156.1:c.570_576del	NP_001138628.1:p.Cys190TrpfsTer?
NM_001145157.1:c.570_576del	NP_001138629.1:p.Cys190TrpfsTer?
NM_001145157.2:c.570_576del	NP_001138629.1:p.Cys190TrpfsTer?
NM_021005.3:c.1029_1035del	NP_066285.1:p.Cys343TrpfsTer?
ENST00000394166.7:c.1029_1035del	ENSP00000377721.3:p.Cys343TrpfsTer?
ENST00000394171.6:c.570_576del	ENSP00000377726.2:p.Cys190TrpfsTer?
ENST00000421109.6:c.630_636del	ENSP00000401674.2:p.Cys210TrpfsTer?
ENST00000453270.2:c.570_576del	ENSP00000389853.2:p.Cys190TrpfsTer?