Canonical Allele Identifier: CA1362363112

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000286G= , CM000665.2:g.47000286G=	GRCh38
NC_000003.11:g.47041776G= , CM000665.1:g.47041776G=	GRCh37
NC_000003.10:g.47016780G=	NCBI36
NG_031914.1:g.25604G= , LRG_568:g.25604G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4187G= MANE Select	ENSP00000415034.2:p.Arg1396=
ENST00000651747.1:c.4085G=	ENSP00000499216.1:p.Arg1362=
ENST00000416683.5:c.2050G=
ENST00000450053.7:c.4187G=	ENSP00000415034.2:p.Arg1396=
NM_015175.2:c.4187G= , LRG_568t1:c.4187G=	NP_055990.1:p.Arg1396=
XM_005264992.2:c.4085G=	XP_005265049.1:p.Arg1362=
XM_005264993.2:c.659G=	XP_005265050.1:p.Arg220=
XM_006713072.2:c.4106G=	XP_006713135.1:p.Arg1369=
XM_011533532.1:c.4166G=	XP_011531834.1:p.Arg1389=
XM_011533533.1:c.4187G=	XP_011531835.1:p.Arg1396=
XM_011533534.1:c.3818G=	XP_011531836.1:p.Arg1273=
XM_011533535.1:c.3647G=	XP_011531837.1:p.Arg1216=
XM_011533536.1:c.3533G=	XP_011531838.1:p.Arg1178=
XM_011533537.1:c.3095G=	XP_011531839.1:p.Arg1032=
XR_940397.1:n.4363G=
XR_940398.1:n.4363G=
NM_001365116.1:c.4085G=	NP_001352045.1:p.Arg1362=
XM_006713072.3:c.4106G=	XP_006713135.1:p.Arg1369=
XM_011533533.2:c.4187G=	XP_011531835.1:p.Arg1396=
XM_017006010.1:c.4187G=	XP_016861499.1:p.Arg1396=
XM_017006011.1:c.4166G=	XP_016861500.1:p.Arg1389=
XM_017006012.1:c.4106G=	XP_016861501.1:p.Arg1369=
XM_017006013.1:c.4187G=	XP_016861502.1:p.Arg1396=
XM_017006014.1:c.4085G=	XP_016861503.1:p.Arg1362=
XM_017006015.1:c.3818G=	XP_016861504.1:p.Arg1273=
XM_017006016.1:c.3647G=	XP_016861505.1:p.Arg1216=
XM_017006017.1:c.659G=	XP_016861506.1:p.Arg220=
XR_940397.2:n.4363G=
NM_001365116.2:c.4085G=	NP_001352045.1:p.Arg1362=
NM_015175.3:c.4187G= MANE Select	NP_055990.1:p.Arg1396=