Canonical Allele Identifier: CA1362363256

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000624_47000625delinsAC , CM000665.2:g.47000624_47000625delinsAC	GRCh38
NC_000003.11:g.47042114_47042115delinsAC , CM000665.1:g.47042114_47042115delinsAC	GRCh37
NC_000003.10:g.47017118_47017119delinsAC	NCBI36
NG_031914.1:g.25942_25943delinsAC , LRG_568:g.25942_25943delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4305+220_4305+221delinsAC MANE Select	ENSP00000415034.2:n.4305+220_4305+221delinsAC
ENST00000651747.1:c.4203+220_4203+221delinsAC	ENSP00000499216.1:n.4203+220_4203+221delinsAC
ENST00000416683.5:c.2168+220_2168+221delinsAC
ENST00000450053.7:c.4305+220_4305+221delinsAC	ENSP00000415034.2:n.4305+220_4305+221delinsAC
NM_015175.2:c.4305+220_4305+221delinsAC , LRG_568t1:c.4305+220_4305+221delinsAC	NP_055990.1:n.4305+220_4305+221delinsAC
XM_005264992.2:c.4203+220_4203+221delinsAC	XP_005265049.1:n.4203+220_4203+221delinsAC
XM_005264993.2:c.777+220_777+221delinsAC	XP_005265050.1:n.777+220_777+221delinsAC
XM_006713072.2:c.4224+220_4224+221delinsAC	XP_006713135.1:n.4224+220_4224+221delinsAC
XM_011533532.1:c.4284+220_4284+221delinsAC	XP_011531834.1:n.4284+220_4284+221delinsAC
XM_011533533.1:c.4305+220_4305+221delinsAC	XP_011531835.1:n.4305+220_4305+221delinsAC
XM_011533534.1:c.3936+220_3936+221delinsAC	XP_011531836.1:n.3936+220_3936+221delinsAC
XM_011533535.1:c.3765+220_3765+221delinsAC	XP_011531837.1:n.3765+220_3765+221delinsAC
XM_011533536.1:c.3651+220_3651+221delinsAC	XP_011531838.1:n.3651+220_3651+221delinsAC
XM_011533537.1:c.3213+220_3213+221delinsAC	XP_011531839.1:n.3213+220_3213+221delinsAC
XR_940397.1:n.4481+220_4481+221delinsAC
XR_940398.1:n.4481+220_4481+221delinsAC
NM_001365116.1:c.4203+220_4203+221delinsAC	NP_001352045.1:n.4203+220_4203+221delinsAC
XM_006713072.3:c.4224+220_4224+221delinsAC	XP_006713135.1:n.4224+220_4224+221delinsAC
XM_011533533.2:c.4305+220_4305+221delinsAC	XP_011531835.1:n.4305+220_4305+221delinsAC
XM_017006010.1:c.4305+220_4305+221delinsAC	XP_016861499.1:n.4305+220_4305+221delinsAC
XM_017006011.1:c.4284+220_4284+221delinsAC	XP_016861500.1:n.4284+220_4284+221delinsAC
XM_017006012.1:c.4224+220_4224+221delinsAC	XP_016861501.1:n.4224+220_4224+221delinsAC
XM_017006013.1:c.4305+220_4305+221delinsAC	XP_016861502.1:n.4305+220_4305+221delinsAC
XM_017006014.1:c.4203+220_4203+221delinsAC	XP_016861503.1:n.4203+220_4203+221delinsAC
XM_017006015.1:c.3936+220_3936+221delinsAC	XP_016861504.1:n.3936+220_3936+221delinsAC
XM_017006016.1:c.3765+220_3765+221delinsAC	XP_016861505.1:n.3765+220_3765+221delinsAC
XM_017006017.1:c.777+220_777+221delinsAC	XP_016861506.1:n.777+220_777+221delinsAC
XR_940397.2:n.4481+220_4481+221delinsAC
NM_001365116.2:c.4203+220_4203+221delinsAC	NP_001352045.1:n.4203+220_4203+221delinsAC
NM_015175.3:c.4305+220_4305+221delinsAC MANE Select	NP_055990.1:n.4305+220_4305+221delinsAC