Canonical Allele Identifier: CA1362363129

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000317C= , CM000665.2:g.47000317C=	GRCh38
NC_000003.11:g.47041807C= , CM000665.1:g.47041807C=	GRCh37
NC_000003.10:g.47016811C=	NCBI36
NG_031914.1:g.25635C= , LRG_568:g.25635C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4218C= MANE Select	ENSP00000415034.2:p.Ser1406=
ENST00000651747.1:c.4116C=	ENSP00000499216.1:p.Ser1372=
ENST00000416683.5:c.2081C=
ENST00000450053.7:c.4218C=	ENSP00000415034.2:p.Ser1406=
NM_015175.2:c.4218C= , LRG_568t1:c.4218C=	NP_055990.1:p.Ser1406=
XM_005264992.2:c.4116C=	XP_005265049.1:p.Ser1372=
XM_005264993.2:c.690C=	XP_005265050.1:p.Ser230=
XM_006713072.2:c.4137C=	XP_006713135.1:p.Ser1379=
XM_011533532.1:c.4197C=	XP_011531834.1:p.Ser1399=
XM_011533533.1:c.4218C=	XP_011531835.1:p.Ser1406=
XM_011533534.1:c.3849C=	XP_011531836.1:p.Ser1283=
XM_011533535.1:c.3678C=	XP_011531837.1:p.Ser1226=
XM_011533536.1:c.3564C=	XP_011531838.1:p.Ser1188=
XM_011533537.1:c.3126C=	XP_011531839.1:p.Ser1042=
XR_940397.1:n.4394C=
XR_940398.1:n.4394C=
NM_001365116.1:c.4116C=	NP_001352045.1:p.Ser1372=
XM_006713072.3:c.4137C=	XP_006713135.1:p.Ser1379=
XM_011533533.2:c.4218C=	XP_011531835.1:p.Ser1406=
XM_017006010.1:c.4218C=	XP_016861499.1:p.Ser1406=
XM_017006011.1:c.4197C=	XP_016861500.1:p.Ser1399=
XM_017006012.1:c.4137C=	XP_016861501.1:p.Ser1379=
XM_017006013.1:c.4218C=	XP_016861502.1:p.Ser1406=
XM_017006014.1:c.4116C=	XP_016861503.1:p.Ser1372=
XM_017006015.1:c.3849C=	XP_016861504.1:p.Ser1283=
XM_017006016.1:c.3678C=	XP_016861505.1:p.Ser1226=
XM_017006017.1:c.690C=	XP_016861506.1:p.Ser230=
XR_940397.2:n.4394C=
NM_001365116.2:c.4116C=	NP_001352045.1:p.Ser1372=
NM_015175.3:c.4218C= MANE Select	NP_055990.1:p.Ser1406=