Canonical Allele Identifier: CA352516319

Gene: NBEAL2

Linked Data

• MyVariant Identifiers: chr3:g.47041491G>C (hg19) ; chr3:g.47000001G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000001G>C , CM000665.2:g.47000001G>C	GRCh38
NC_000003.11:g.47041491G>C , CM000665.1:g.47041491G>C	GRCh37
NC_000003.10:g.47016495G>C	NCBI36
NG_031914.1:g.25319G>C , LRG_568:g.25319G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.3902G>C MANE Select	ENSP00000415034.2:p.Ser1301Thr
ENST00000651747.1:c.3800G>C	ENSP00000499216.1:p.Ser1267Thr
ENST00000652744.1:n.239G>C
ENST00000416683.5:c.1960-195G>C
ENST00000450053.7:c.3902G>C	ENSP00000415034.2:p.Ser1301Thr
NM_015175.2:c.3902G>C , LRG_568t1:c.3902G>C	NP_055990.1:p.Ser1301Thr
XM_005264992.2:c.3800G>C	XP_005265049.1:p.Ser1267Thr
XM_005264993.2:c.374G>C	XP_005265050.1:p.Ser125Thr
XM_006713072.2:c.3821G>C	XP_006713135.1:p.Ser1274Thr
XM_011533532.1:c.3881G>C	XP_011531834.1:p.Ser1294Thr
XM_011533533.1:c.3902G>C	XP_011531835.1:p.Ser1301Thr
XM_011533534.1:c.3533G>C	XP_011531836.1:p.Ser1178Thr
XM_011533535.1:c.3362G>C	XP_011531837.1:p.Ser1121Thr
XM_011533536.1:c.3248G>C	XP_011531838.1:p.Ser1083Thr
XM_011533537.1:c.2810G>C	XP_011531839.1:p.Ser937Thr
XR_940397.1:n.4078G>C
XR_940398.1:n.4078G>C
NM_001365116.1:c.3800G>C	NP_001352045.1:p.Ser1267Thr
XM_006713072.3:c.3821G>C	XP_006713135.1:p.Ser1274Thr
XM_011533533.2:c.3902G>C	XP_011531835.1:p.Ser1301Thr
XM_017006010.1:c.3902G>C	XP_016861499.1:p.Ser1301Thr
XM_017006011.1:c.3881G>C	XP_016861500.1:p.Ser1294Thr
XM_017006012.1:c.3821G>C	XP_016861501.1:p.Ser1274Thr
XM_017006013.1:c.3902G>C	XP_016861502.1:p.Ser1301Thr
XM_017006014.1:c.3800G>C	XP_016861503.1:p.Ser1267Thr
XM_017006015.1:c.3533G>C	XP_016861504.1:p.Ser1178Thr
XM_017006016.1:c.3362G>C	XP_016861505.1:p.Ser1121Thr
XM_017006017.1:c.374G>C	XP_016861506.1:p.Ser125Thr
XR_940397.2:n.4078G>C
NM_001365116.2:c.3800G>C	NP_001352045.1:p.Ser1267Thr
NM_015175.3:c.3902G>C MANE Select	NP_055990.1:p.Ser1301Thr