Canonical Allele Identifier: CA356725140

Gene: N4BP2

Linked Data

• MyVariant Identifiers: chr4:g.40123392T>A (hg19) ; chr4:g.40121772T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40121772T>A , CM000666.2:g.40121772T>A	GRCh38
NC_000004.11:g.40123392T>A , CM000666.1:g.40123392T>A	GRCh37
NC_000004.10:g.39799787T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706658.1:c.*3452T>A	ENSP00000516486.1:n.*3452T>A
ENST00000261435.11:c.3661T>A MANE Select	ENSP00000261435.6:p.Phe1221Ile
ENST00000261435.10:c.3661T>A	ENSP00000261435.6:p.Phe1221Ile
ENST00000511480.5:c.*3452T>A	ENSP00000422436.1:n.*3452T>A
ENST00000513269.1:c.2600T>A
NM_018177.4:c.3661T>A	NP_060647.2:p.Phe1221Ile
XM_006714022.2:c.3421T>A	XP_006714085.1:p.Phe1141Ile
XM_006714023.2:c.3421T>A	XP_006714086.1:p.Phe1141Ile
XM_011513715.1:c.4057T>A	XP_011512017.1:p.Phe1353Ile
XM_011513716.1:c.4057T>A	XP_011512018.1:p.Phe1353Ile
XM_011513717.1:c.4057T>A	XP_011512019.1:p.Phe1353Ile
XM_011513718.1:c.3661T>A	XP_011512020.1:p.Phe1221Ile
XM_011513719.1:c.3421T>A	XP_011512021.1:p.Phe1141Ile
XM_011513720.1:c.3421T>A	XP_011512022.1:p.Phe1141Ile
XM_011513721.1:c.3421T>A	XP_011512023.1:p.Phe1141Ile
NM_001318359.1:c.3421T>A	NP_001305288.1:p.Phe1141Ile
NM_018177.5:c.3661T>A	NP_060647.2:p.Phe1221Ile
XM_006714023.3:c.3421T>A	XP_006714086.1:p.Phe1141Ile
XM_011513716.2:c.4057T>A	XP_011512018.1:p.Phe1353Ile
XM_011513717.2:c.4057T>A	XP_011512019.1:p.Phe1353Ile
XM_011513718.2:c.3661T>A	XP_011512020.1:p.Phe1221Ile
XM_011513719.2:c.3421T>A	XP_011512021.1:p.Phe1141Ile
XM_017008397.1:c.4057T>A	XP_016863886.1:p.Phe1353Ile
XM_017008398.1:c.3661T>A	XP_016863887.1:p.Phe1221Ile
XM_017008399.1:c.3421T>A	XP_016863888.1:p.Phe1141Ile
XR_001741283.1:n.4238T>A
NM_018177.6:c.3661T>A MANE Select	NP_060647.2:p.Phe1221Ile
NM_001318359.2:c.3421T>A	NP_001305288.1:p.Phe1141Ile