Canonical Allele Identifier: CA352517062

Gene: NBEAL2

Linked Data

• MyVariant Identifiers: chr3:g.47041767A>T (hg19) ; chr3:g.47000277A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000277A>T , CM000665.2:g.47000277A>T	GRCh38
NC_000003.11:g.47041767A>T , CM000665.1:g.47041767A>T	GRCh37
NC_000003.10:g.47016771A>T	NCBI36
NG_031914.1:g.25595A>T , LRG_568:g.25595A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000450053.8:c.4178A>T MANE Select	ENSP00000415034.2:p.Asp1393Val
ENST00000651747.1:c.4076A>T	ENSP00000499216.1:p.Asp1359Val
ENST00000416683.5:c.2041A>T
ENST00000450053.7:c.4178A>T	ENSP00000415034.2:p.Asp1393Val
NM_015175.2:c.4178A>T , LRG_568t1:c.4178A>T	NP_055990.1:p.Asp1393Val
XM_005264992.2:c.4076A>T	XP_005265049.1:p.Asp1359Val
XM_005264993.2:c.650A>T	XP_005265050.1:p.Asp217Val
XM_006713072.2:c.4097A>T	XP_006713135.1:p.Asp1366Val
XM_011533532.1:c.4157A>T	XP_011531834.1:p.Asp1386Val
XM_011533533.1:c.4178A>T	XP_011531835.1:p.Asp1393Val
XM_011533534.1:c.3809A>T	XP_011531836.1:p.Asp1270Val
XM_011533535.1:c.3638A>T	XP_011531837.1:p.Asp1213Val
XM_011533536.1:c.3524A>T	XP_011531838.1:p.Asp1175Val
XM_011533537.1:c.3086A>T	XP_011531839.1:p.Asp1029Val
XR_940397.1:n.4354A>T
XR_940398.1:n.4354A>T
NM_001365116.1:c.4076A>T	NP_001352045.1:p.Asp1359Val
XM_006713072.3:c.4097A>T	XP_006713135.1:p.Asp1366Val
XM_011533533.2:c.4178A>T	XP_011531835.1:p.Asp1393Val
XM_017006010.1:c.4178A>T	XP_016861499.1:p.Asp1393Val
XM_017006011.1:c.4157A>T	XP_016861500.1:p.Asp1386Val
XM_017006012.1:c.4097A>T	XP_016861501.1:p.Asp1366Val
XM_017006013.1:c.4178A>T	XP_016861502.1:p.Asp1393Val
XM_017006014.1:c.4076A>T	XP_016861503.1:p.Asp1359Val
XM_017006015.1:c.3809A>T	XP_016861504.1:p.Asp1270Val
XM_017006016.1:c.3638A>T	XP_016861505.1:p.Asp1213Val
XM_017006017.1:c.650A>T	XP_016861506.1:p.Asp217Val
XR_940397.2:n.4354A>T
NM_001365116.2:c.4076A>T	NP_001352045.1:p.Asp1359Val
NM_015175.3:c.4178A>T MANE Select	NP_055990.1:p.Asp1393Val