Canonical Allele Identifier: CA1362363089

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000256C= , CM000665.2:g.47000256C=	GRCh38
NC_000003.11:g.47041746C= , CM000665.1:g.47041746C=	GRCh37
NC_000003.10:g.47016750C=	NCBI36
NG_031914.1:g.25574C= , LRG_568:g.25574C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4157C= MANE Select	ENSP00000415034.2:p.Pro1386=
ENST00000651747.1:c.4055C=	ENSP00000499216.1:p.Pro1352=
ENST00000416683.5:c.2020C=
ENST00000450053.7:c.4157C=	ENSP00000415034.2:p.Pro1386=
NM_015175.2:c.4157C= , LRG_568t1:c.4157C=	NP_055990.1:p.Pro1386=
XM_005264992.2:c.4055C=	XP_005265049.1:p.Pro1352=
XM_005264993.2:c.629C=	XP_005265050.1:p.Pro210=
XM_006713072.2:c.4076C=	XP_006713135.1:p.Pro1359=
XM_011533532.1:c.4136C=	XP_011531834.1:p.Pro1379=
XM_011533533.1:c.4157C=	XP_011531835.1:p.Pro1386=
XM_011533534.1:c.3788C=	XP_011531836.1:p.Pro1263=
XM_011533535.1:c.3617C=	XP_011531837.1:p.Pro1206=
XM_011533536.1:c.3503C=	XP_011531838.1:p.Pro1168=
XM_011533537.1:c.3065C=	XP_011531839.1:p.Pro1022=
XR_940397.1:n.4333C=
XR_940398.1:n.4333C=
NM_001365116.1:c.4055C=	NP_001352045.1:p.Pro1352=
XM_006713072.3:c.4076C=	XP_006713135.1:p.Pro1359=
XM_011533533.2:c.4157C=	XP_011531835.1:p.Pro1386=
XM_017006010.1:c.4157C=	XP_016861499.1:p.Pro1386=
XM_017006011.1:c.4136C=	XP_016861500.1:p.Pro1379=
XM_017006012.1:c.4076C=	XP_016861501.1:p.Pro1359=
XM_017006013.1:c.4157C=	XP_016861502.1:p.Pro1386=
XM_017006014.1:c.4055C=	XP_016861503.1:p.Pro1352=
XM_017006015.1:c.3788C=	XP_016861504.1:p.Pro1263=
XM_017006016.1:c.3617C=	XP_016861505.1:p.Pro1206=
XM_017006017.1:c.629C=	XP_016861506.1:p.Pro210=
XR_940397.2:n.4333C=
NM_001365116.2:c.4055C=	NP_001352045.1:p.Pro1352=
NM_015175.3:c.4157C= MANE Select	NP_055990.1:p.Pro1386=