Canonical Allele Identifier: CA1362363266

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000646C= , CM000665.2:g.47000646C=	GRCh38
NC_000003.11:g.47042136C= , CM000665.1:g.47042136C=	GRCh37
NC_000003.10:g.47017140C=	NCBI36
NG_031914.1:g.25964C= , LRG_568:g.25964C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4305+242C= MANE Select	ENSP00000415034.2:n.4305+242C=
ENST00000651747.1:c.4203+242C=	ENSP00000499216.1:n.4203+242C=
ENST00000416683.5:c.2168+242C=
ENST00000450053.7:c.4305+242C=	ENSP00000415034.2:n.4305+242C=
NM_015175.2:c.4305+242C= , LRG_568t1:c.4305+242C=	NP_055990.1:n.4305+242C=
XM_005264992.2:c.4203+242C=	XP_005265049.1:n.4203+242C=
XM_005264993.2:c.777+242C=	XP_005265050.1:n.777+242C=
XM_006713072.2:c.4224+242C=	XP_006713135.1:n.4224+242C=
XM_011533532.1:c.4284+242C=	XP_011531834.1:n.4284+242C=
XM_011533533.1:c.4305+242C=	XP_011531835.1:n.4305+242C=
XM_011533534.1:c.3936+242C=	XP_011531836.1:n.3936+242C=
XM_011533535.1:c.3765+242C=	XP_011531837.1:n.3765+242C=
XM_011533536.1:c.3651+242C=	XP_011531838.1:n.3651+242C=
XM_011533537.1:c.3213+242C=	XP_011531839.1:n.3213+242C=
XR_940397.1:n.4481+242C=
XR_940398.1:n.4481+242C=
NM_001365116.1:c.4203+242C=	NP_001352045.1:n.4203+242C=
XM_006713072.3:c.4224+242C=	XP_006713135.1:n.4224+242C=
XM_011533533.2:c.4305+242C=	XP_011531835.1:n.4305+242C=
XM_017006010.1:c.4305+242C=	XP_016861499.1:n.4305+242C=
XM_017006011.1:c.4284+242C=	XP_016861500.1:n.4284+242C=
XM_017006012.1:c.4224+242C=	XP_016861501.1:n.4224+242C=
XM_017006013.1:c.4305+242C=	XP_016861502.1:n.4305+242C=
XM_017006014.1:c.4203+242C=	XP_016861503.1:n.4203+242C=
XM_017006015.1:c.3936+242C=	XP_016861504.1:n.3936+242C=
XM_017006016.1:c.3765+242C=	XP_016861505.1:n.3765+242C=
XM_017006017.1:c.777+242C=	XP_016861506.1:n.777+242C=
XR_940397.2:n.4481+242C=
NM_001365116.2:c.4203+242C=	NP_001352045.1:n.4203+242C=
NM_015175.3:c.4305+242C= MANE Select	NP_055990.1:n.4305+242C=