Canonical Allele Identifier: CA1362363015

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000092C= , CM000665.2:g.47000092C=	GRCh38
NC_000003.11:g.47041582C= , CM000665.1:g.47041582C=	GRCh37
NC_000003.10:g.47016586C=	NCBI36
NG_031914.1:g.25410C= , LRG_568:g.25410C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.3993C= MANE Select	ENSP00000415034.2:p.Val1331=
ENST00000651747.1:c.3891C=	ENSP00000499216.1:p.Val1297=
ENST00000652744.1:n.330C=
ENST00000416683.5:c.1960-104C=
ENST00000450053.7:c.3993C=	ENSP00000415034.2:p.Val1331=
NM_015175.2:c.3993C= , LRG_568t1:c.3993C=	NP_055990.1:p.Val1331=
XM_005264992.2:c.3891C=	XP_005265049.1:p.Val1297=
XM_005264993.2:c.465C=	XP_005265050.1:p.Val155=
XM_006713072.2:c.3912C=	XP_006713135.1:p.Val1304=
XM_011533532.1:c.3972C=	XP_011531834.1:p.Val1324=
XM_011533533.1:c.3993C=	XP_011531835.1:p.Val1331=
XM_011533534.1:c.3624C=	XP_011531836.1:p.Val1208=
XM_011533535.1:c.3453C=	XP_011531837.1:p.Val1151=
XM_011533536.1:c.3339C=	XP_011531838.1:p.Val1113=
XM_011533537.1:c.2901C=	XP_011531839.1:p.Val967=
XR_940397.1:n.4169C=
XR_940398.1:n.4169C=
NM_001365116.1:c.3891C=	NP_001352045.1:p.Val1297=
XM_006713072.3:c.3912C=	XP_006713135.1:p.Val1304=
XM_011533533.2:c.3993C=	XP_011531835.1:p.Val1331=
XM_017006010.1:c.3993C=	XP_016861499.1:p.Val1331=
XM_017006011.1:c.3972C=	XP_016861500.1:p.Val1324=
XM_017006012.1:c.3912C=	XP_016861501.1:p.Val1304=
XM_017006013.1:c.3993C=	XP_016861502.1:p.Val1331=
XM_017006014.1:c.3891C=	XP_016861503.1:p.Val1297=
XM_017006015.1:c.3624C=	XP_016861504.1:p.Val1208=
XM_017006016.1:c.3453C=	XP_016861505.1:p.Val1151=
XM_017006017.1:c.465C=	XP_016861506.1:p.Val155=
XR_940397.2:n.4169C=
NM_001365116.2:c.3891C=	NP_001352045.1:p.Val1297=
NM_015175.3:c.3993C= MANE Select	NP_055990.1:p.Val1331=