Canonical Allele Identifier: CA352516795

Gene: NBEAL2

Linked Data

• MyVariant Identifiers: chr3:g.47041631G>C (hg19) ; chr3:g.47000141G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000141G>C , CM000665.2:g.47000141G>C	GRCh38
NC_000003.11:g.47041631G>C , CM000665.1:g.47041631G>C	GRCh37
NC_000003.10:g.47016635G>C	NCBI36
NG_031914.1:g.25459G>C , LRG_568:g.25459G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4042G>C MANE Select	ENSP00000415034.2:p.Ala1348Pro
ENST00000651747.1:c.3940G>C	ENSP00000499216.1:p.Ala1314Pro
ENST00000652744.1:n.379G>C
ENST00000416683.5:c.1960-55G>C
ENST00000450053.7:c.4042G>C	ENSP00000415034.2:p.Ala1348Pro
NM_015175.2:c.4042G>C , LRG_568t1:c.4042G>C	NP_055990.1:p.Ala1348Pro
XM_005264992.2:c.3940G>C	XP_005265049.1:p.Ala1314Pro
XM_005264993.2:c.514G>C	XP_005265050.1:p.Ala172Pro
XM_006713072.2:c.3961G>C	XP_006713135.1:p.Ala1321Pro
XM_011533532.1:c.4021G>C	XP_011531834.1:p.Ala1341Pro
XM_011533533.1:c.4042G>C	XP_011531835.1:p.Ala1348Pro
XM_011533534.1:c.3673G>C	XP_011531836.1:p.Ala1225Pro
XM_011533535.1:c.3502G>C	XP_011531837.1:p.Ala1168Pro
XM_011533536.1:c.3388G>C	XP_011531838.1:p.Ala1130Pro
XM_011533537.1:c.2950G>C	XP_011531839.1:p.Ala984Pro
XR_940397.1:n.4218G>C
XR_940398.1:n.4218G>C
NM_001365116.1:c.3940G>C	NP_001352045.1:p.Ala1314Pro
XM_006713072.3:c.3961G>C	XP_006713135.1:p.Ala1321Pro
XM_011533533.2:c.4042G>C	XP_011531835.1:p.Ala1348Pro
XM_017006010.1:c.4042G>C	XP_016861499.1:p.Ala1348Pro
XM_017006011.1:c.4021G>C	XP_016861500.1:p.Ala1341Pro
XM_017006012.1:c.3961G>C	XP_016861501.1:p.Ala1321Pro
XM_017006013.1:c.4042G>C	XP_016861502.1:p.Ala1348Pro
XM_017006014.1:c.3940G>C	XP_016861503.1:p.Ala1314Pro
XM_017006015.1:c.3673G>C	XP_016861504.1:p.Ala1225Pro
XM_017006016.1:c.3502G>C	XP_016861505.1:p.Ala1168Pro
XM_017006017.1:c.514G>C	XP_016861506.1:p.Ala172Pro
XR_940397.2:n.4218G>C
NM_001365116.2:c.3940G>C	NP_001352045.1:p.Ala1314Pro
NM_015175.3:c.4042G>C MANE Select	NP_055990.1:p.Ala1348Pro