Canonical Allele Identifier: CA352516838

Gene: NBEAL2

Linked Data

• MyVariant Identifiers: chr3:g.47041652C>G (hg19) ; chr3:g.47000162C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.47000162C>G , CM000665.2:g.47000162C>G	GRCh38
NC_000003.11:g.47041652C>G , CM000665.1:g.47041652C>G	GRCh37
NC_000003.10:g.47016656C>G	NCBI36
NG_031914.1:g.25480C>G , LRG_568:g.25480C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000450053.8:c.4063C>G MANE Select	ENSP00000415034.2:p.Pro1355Ala
ENST00000651747.1:c.3961C>G	ENSP00000499216.1:p.Pro1321Ala
ENST00000652744.1:n.400C>G
ENST00000416683.5:c.1960-34C>G
ENST00000450053.7:c.4063C>G	ENSP00000415034.2:p.Pro1355Ala
NM_015175.2:c.4063C>G , LRG_568t1:c.4063C>G	NP_055990.1:p.Pro1355Ala
XM_005264992.2:c.3961C>G	XP_005265049.1:p.Pro1321Ala
XM_005264993.2:c.535C>G	XP_005265050.1:p.Pro179Ala
XM_006713072.2:c.3982C>G	XP_006713135.1:p.Pro1328Ala
XM_011533532.1:c.4042C>G	XP_011531834.1:p.Pro1348Ala
XM_011533533.1:c.4063C>G	XP_011531835.1:p.Pro1355Ala
XM_011533534.1:c.3694C>G	XP_011531836.1:p.Pro1232Ala
XM_011533535.1:c.3523C>G	XP_011531837.1:p.Pro1175Ala
XM_011533536.1:c.3409C>G	XP_011531838.1:p.Pro1137Ala
XM_011533537.1:c.2971C>G	XP_011531839.1:p.Pro991Ala
XR_940397.1:n.4239C>G
XR_940398.1:n.4239C>G
NM_001365116.1:c.3961C>G	NP_001352045.1:p.Pro1321Ala
XM_006713072.3:c.3982C>G	XP_006713135.1:p.Pro1328Ala
XM_011533533.2:c.4063C>G	XP_011531835.1:p.Pro1355Ala
XM_017006010.1:c.4063C>G	XP_016861499.1:p.Pro1355Ala
XM_017006011.1:c.4042C>G	XP_016861500.1:p.Pro1348Ala
XM_017006012.1:c.3982C>G	XP_016861501.1:p.Pro1328Ala
XM_017006013.1:c.4063C>G	XP_016861502.1:p.Pro1355Ala
XM_017006014.1:c.3961C>G	XP_016861503.1:p.Pro1321Ala
XM_017006015.1:c.3694C>G	XP_016861504.1:p.Pro1232Ala
XM_017006016.1:c.3523C>G	XP_016861505.1:p.Pro1175Ala
XM_017006017.1:c.535C>G	XP_016861506.1:p.Pro179Ala
XR_940397.2:n.4239C>G
NM_001365116.2:c.3961C>G	NP_001352045.1:p.Pro1321Ala
NM_015175.3:c.4063C>G MANE Select	NP_055990.1:p.Pro1355Ala