Canonical Allele Identifier: CA2361899

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47005519G>C , CM000665.2:g.47005519G>C	GRCh38
NC_000003.11:g.47047009G>C , CM000665.1:g.47047009G>C	GRCh37
NC_000003.10:g.47022013G>C	NCBI36
NG_031914.1:g.30837G>C , LRG_568:g.30837G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_015175.3:c.6591G>C MANE Select	NP_055990.1:p.Ser2197=
ENST00000450053.8:c.6591G>C MANE Select	ENSP00000415034.2:p.Ser2197=
NM_001365116.1:c.6489G>C	NP_001352045.1:p.Ser2163=
NM_001365116.2:c.6489G>C	NP_001352045.1:p.Ser2163=
NM_015175.2:c.6591G>C , LRG_568t1:c.6591G>C	NP_055990.1:p.Ser2197=
ENST00000416683.5:c.4454G>C
ENST00000423436.1:c.72G>C	ENSP00000415063.1:p.Ser24=
ENST00000441027.5:c.490G>C	ENSP00000409601.1:n.490G>C
ENST00000443829.5:c.1696G>C
ENST00000450053.7:c.6591G>C	ENSP00000415034.2:p.Ser2197=
ENST00000486870.1:n.650G>C
ENST00000651453.1:n.376G>C
ENST00000651747.1:c.6489G>C	ENSP00000499216.1:p.Ser2163=
XM_005264992.2:c.6489G>C	XP_005265049.1:p.Ser2163=
XM_005264993.2:c.3063G>C	XP_005265050.1:p.Ser1021=
XM_006713072.2:c.6510G>C	XP_006713135.1:p.Ser2170=
XM_006713072.3:c.6510G>C	XP_006713135.1:p.Ser2170=
XM_011533532.1:c.6570G>C	XP_011531834.1:p.Ser2190=
XM_011533533.1:c.6591G>C	XP_011531835.1:p.Ser2197=
XM_011533533.2:c.6591G>C	XP_011531835.1:p.Ser2197=
XM_011533534.1:c.6222G>C	XP_011531836.1:p.Ser2074=
XM_011533535.1:c.6051G>C	XP_011531837.1:p.Ser2017=
XM_011533536.1:c.5937G>C	XP_011531838.1:p.Ser1979=
XM_011533537.1:c.5499G>C	XP_011531839.1:p.Ser1833=
XM_017006010.1:c.6591G>C	XP_016861499.1:p.Ser2197=
XM_017006011.1:c.6570G>C	XP_016861500.1:p.Ser2190=
XM_017006012.1:c.6510G>C	XP_016861501.1:p.Ser2170=
XM_017006013.1:c.6591G>C	XP_016861502.1:p.Ser2197=
XM_017006014.1:c.6489G>C	XP_016861503.1:p.Ser2163=
XM_017006015.1:c.6222G>C	XP_016861504.1:p.Ser2074=
XM_017006016.1:c.6051G>C	XP_016861505.1:p.Ser2017=
XM_017006017.1:c.3063G>C	XP_016861506.1:p.Ser1021=
XR_940397.1:n.6767G>C
XR_940397.2:n.6767G>C