Canonical Allele Identifier: CA433598385

Gene: NBEAL2

Linked Data

• COSMIC: COSM5965746
• MyVariant Identifiers: chr3:g.47041645C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000155C>T , CM000665.2:g.47000155C>T	GRCh38
NC_000003.11:g.47041645C>T , CM000665.1:g.47041645C>T	GRCh37
NC_000003.10:g.47016649C>T	NCBI36
NG_031914.1:g.25473C>T , LRG_568:g.25473C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4056C>T MANE Select	ENSP00000415034.2:p.Phe1352=
ENST00000651747.1:c.3954C>T	ENSP00000499216.1:p.Phe1318=
ENST00000652744.1:n.393C>T
ENST00000416683.5:c.1960-41C>T
ENST00000450053.7:c.4056C>T	ENSP00000415034.2:p.Phe1352=
NM_015175.2:c.4056C>T , LRG_568t1:c.4056C>T	NP_055990.1:p.Phe1352=
XM_005264992.2:c.3954C>T	XP_005265049.1:p.Phe1318=
XM_005264993.2:c.528C>T	XP_005265050.1:p.Phe176=
XM_006713072.2:c.3975C>T	XP_006713135.1:p.Phe1325=
XM_011533532.1:c.4035C>T	XP_011531834.1:p.Phe1345=
XM_011533533.1:c.4056C>T	XP_011531835.1:p.Phe1352=
XM_011533534.1:c.3687C>T	XP_011531836.1:p.Phe1229=
XM_011533535.1:c.3516C>T	XP_011531837.1:p.Phe1172=
XM_011533536.1:c.3402C>T	XP_011531838.1:p.Phe1134=
XM_011533537.1:c.2964C>T	XP_011531839.1:p.Phe988=
XR_940397.1:n.4232C>T
XR_940398.1:n.4232C>T
NM_001365116.1:c.3954C>T	NP_001352045.1:p.Phe1318=
XM_006713072.3:c.3975C>T	XP_006713135.1:p.Phe1325=
XM_011533533.2:c.4056C>T	XP_011531835.1:p.Phe1352=
XM_017006010.1:c.4056C>T	XP_016861499.1:p.Phe1352=
XM_017006011.1:c.4035C>T	XP_016861500.1:p.Phe1345=
XM_017006012.1:c.3975C>T	XP_016861501.1:p.Phe1325=
XM_017006013.1:c.4056C>T	XP_016861502.1:p.Phe1352=
XM_017006014.1:c.3954C>T	XP_016861503.1:p.Phe1318=
XM_017006015.1:c.3687C>T	XP_016861504.1:p.Phe1229=
XM_017006016.1:c.3516C>T	XP_016861505.1:p.Phe1172=
XM_017006017.1:c.528C>T	XP_016861506.1:p.Phe176=
XR_940397.2:n.4232C>T
NM_001365116.2:c.3954C>T	NP_001352045.1:p.Phe1318=
NM_015175.3:c.4056C>T MANE Select	NP_055990.1:p.Phe1352=