Canonical Allele Identifier: CA2360902

Gene: NBEAL2

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46998786G>A , CM000665.2:g.46998786G>A	GRCh38
NC_000003.11:g.47040276G>A , CM000665.1:g.47040276G>A	GRCh37
NC_000003.10:g.47015280G>A	NCBI36
NG_031914.1:g.24104G>A , LRG_568:g.24104G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_015175.3:c.3291G>A MANE Select	NP_055990.1:p.Ala1097=
ENST00000450053.8:c.3291G>A MANE Select	ENSP00000415034.2:p.Ala1097=
NM_001365116.1:c.3189G>A	NP_001352045.1:p.Ala1063=
NM_001365116.2:c.3189G>A	NP_001352045.1:p.Ala1063=
NM_015175.2:c.3291G>A , LRG_568t1:c.3291G>A	NP_055990.1:p.Ala1097=
ENST00000416683.5:c.1706G>A
ENST00000450053.7:c.3291G>A	ENSP00000415034.2:p.Ala1097=
ENST00000651747.1:c.3189G>A	ENSP00000499216.1:p.Ala1063=
XM_005264992.2:c.3189G>A	XP_005265049.1:p.Ala1063=
XM_006713072.2:c.3210G>A	XP_006713135.1:p.Ala1070=
XM_006713072.3:c.3210G>A	XP_006713135.1:p.Ala1070=
XM_011533532.1:c.3270G>A	XP_011531834.1:p.Ala1090=
XM_011533533.1:c.3291G>A	XP_011531835.1:p.Ala1097=
XM_011533533.2:c.3291G>A	XP_011531835.1:p.Ala1097=
XM_011533534.1:c.2922G>A	XP_011531836.1:p.Ala974=
XM_011533535.1:c.2751G>A	XP_011531837.1:p.Ala917=
XM_011533536.1:c.2637G>A	XP_011531838.1:p.Ala879=
XM_011533537.1:c.2199G>A	XP_011531839.1:p.Ala733=
XM_017006010.1:c.3291G>A	XP_016861499.1:p.Ala1097=
XM_017006011.1:c.3270G>A	XP_016861500.1:p.Ala1090=
XM_017006012.1:c.3210G>A	XP_016861501.1:p.Ala1070=
XM_017006013.1:c.3291G>A	XP_016861502.1:p.Ala1097=
XM_017006014.1:c.3189G>A	XP_016861503.1:p.Ala1063=
XM_017006015.1:c.2922G>A	XP_016861504.1:p.Ala974=
XM_017006016.1:c.2751G>A	XP_016861505.1:p.Ala917=
XR_940397.1:n.3467G>A
XR_940397.2:n.3467G>A
XR_940398.1:n.3467G>A