Canonical Allele Identifier: CA2674596829

Gene: NR2F1

Linked Data

• gnomAD v4: 5-93585499-T-TCCCTA

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.93585500_93585501insCCTAC , CM000667.2:g.93585500_93585501insCCTAC	GRCh38
NC_000005.9:g.92921206_92921207insCCTAC , CM000667.1:g.92921206_92921207insCCTAC	GRCh37
NC_000005.8:g.92946962_92946963insCCTAC	NCBI36
NG_034119.1:g.7164_7165insCCTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615873.2:c.388+14_388+15insCCTAC	ENSP00000481517.1:n.388+14_388+15insCCTAC
ENST00000327111.8:c.463+14_463+15insCCTAC MANE Select	ENSP00000325819.3:n.463+14_463+15insCCTAC
ENST00000647447.1:c.310+14_310+15insCCTAC	ENSP00000495740.1:n.310+14_310+15insCCTAC
ENST00000327111.7:c.463+14_463+15insCCTAC	ENSP00000325819.3:n.463+14_463+15insCCTAC
ENST00000615873.1:c.388+14_388+15insCCTAC	ENSP00000481517.1:n.388+14_388+15insCCTAC
NM_005654.5:c.463+14_463+15insCCTAC	NP_005645.1:n.463+14_463+15insCCTAC
NM_005654.6:c.463+14_463+15insCCTAC MANE Select	NP_005645.1:n.463+14_463+15insCCTAC