Canonical Allele Identifier: CA352527595

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47003872G>A , CM000665.2:g.47003872G>A	GRCh38
NC_000003.11:g.47045362G>A , CM000665.1:g.47045362G>A	GRCh37
NC_000003.10:g.47020366G>A	NCBI36
NG_031914.1:g.29190G>A , LRG_568:g.29190G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015175.3:c.5777G>A MANE Select	NP_055990.1:p.Cys1926Tyr
ENST00000450053.8:c.5777G>A MANE Select	ENSP00000415034.2:p.Cys1926Tyr
NM_001365116.1:c.5675G>A	NP_001352045.1:p.Cys1892Tyr
NM_001365116.2:c.5675G>A	NP_001352045.1:p.Cys1892Tyr
NM_015175.2:c.5777G>A , LRG_568t1:c.5777G>A	NP_055990.1:p.Cys1926Tyr
ENST00000416683.5:c.3640G>A
ENST00000443829.5:c.882G>A
ENST00000450053.7:c.5777G>A	ENSP00000415034.2:p.Cys1926Tyr
ENST00000651747.1:c.5675G>A	ENSP00000499216.1:p.Cys1892Tyr
XM_005264992.2:c.5675G>A	XP_005265049.1:p.Cys1892Tyr
XM_005264993.2:c.2249G>A	XP_005265050.1:p.Cys750Tyr
XM_006713072.2:c.5696G>A	XP_006713135.1:p.Cys1899Tyr
XM_006713072.3:c.5696G>A	XP_006713135.1:p.Cys1899Tyr
XM_011533532.1:c.5756G>A	XP_011531834.1:p.Cys1919Tyr
XM_011533533.1:c.5777G>A	XP_011531835.1:p.Cys1926Tyr
XM_011533533.2:c.5777G>A	XP_011531835.1:p.Cys1926Tyr
XM_011533534.1:c.5408G>A	XP_011531836.1:p.Cys1803Tyr
XM_011533535.1:c.5237G>A	XP_011531837.1:p.Cys1746Tyr
XM_011533536.1:c.5123G>A	XP_011531838.1:p.Cys1708Tyr
XM_011533537.1:c.4685G>A	XP_011531839.1:p.Cys1562Tyr
XM_017006010.1:c.5777G>A	XP_016861499.1:p.Cys1926Tyr
XM_017006011.1:c.5756G>A	XP_016861500.1:p.Cys1919Tyr
XM_017006012.1:c.5696G>A	XP_016861501.1:p.Cys1899Tyr
XM_017006013.1:c.5777G>A	XP_016861502.1:p.Cys1926Tyr
XM_017006014.1:c.5675G>A	XP_016861503.1:p.Cys1892Tyr
XM_017006015.1:c.5408G>A	XP_016861504.1:p.Cys1803Tyr
XM_017006016.1:c.5237G>A	XP_016861505.1:p.Cys1746Tyr
XM_017006017.1:c.2249G>A	XP_016861506.1:p.Cys750Tyr
XR_940397.1:n.5953G>A
XR_940397.2:n.5953G>A