Canonical Allele Identifier: CA1452455636

Gene: N4BP2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40121784G= , CM000666.2:g.40121784G=	GRCh38
NC_000004.11:g.40123404G= , CM000666.1:g.40123404G=	GRCh37
NC_000004.10:g.39799799G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706658.1:c.*3464G=	ENSP00000516486.1:n.*3464G=
ENST00000261435.11:c.3673G= MANE Select	ENSP00000261435.6:p.Ala1225=
ENST00000261435.10:c.3673G=	ENSP00000261435.6:p.Ala1225=
ENST00000511480.5:c.*3464G=	ENSP00000422436.1:n.*3464G=
ENST00000513269.1:c.2612G=
NM_018177.4:c.3673G=	NP_060647.2:p.Ala1225=
XM_006714022.2:c.3433G=	XP_006714085.1:p.Ala1145=
XM_006714023.2:c.3433G=	XP_006714086.1:p.Ala1145=
XM_011513715.1:c.4069G=	XP_011512017.1:p.Ala1357=
XM_011513716.1:c.4069G=	XP_011512018.1:p.Ala1357=
XM_011513717.1:c.4069G=	XP_011512019.1:p.Ala1357=
XM_011513718.1:c.3673G=	XP_011512020.1:p.Ala1225=
XM_011513719.1:c.3433G=	XP_011512021.1:p.Ala1145=
XM_011513720.1:c.3433G=	XP_011512022.1:p.Ala1145=
XM_011513721.1:c.3433G=	XP_011512023.1:p.Ala1145=
NM_001318359.1:c.3433G=	NP_001305288.1:p.Ala1145=
NM_018177.5:c.3673G=	NP_060647.2:p.Ala1225=
XM_006714023.3:c.3433G=	XP_006714086.1:p.Ala1145=
XM_011513716.2:c.4069G=	XP_011512018.1:p.Ala1357=
XM_011513717.2:c.4069G=	XP_011512019.1:p.Ala1357=
XM_011513718.2:c.3673G=	XP_011512020.1:p.Ala1225=
XM_011513719.2:c.3433G=	XP_011512021.1:p.Ala1145=
XM_017008397.1:c.4069G=	XP_016863886.1:p.Ala1357=
XM_017008398.1:c.3673G=	XP_016863887.1:p.Ala1225=
XM_017008399.1:c.3433G=	XP_016863888.1:p.Ala1145=
XR_001741283.1:n.4250G=
NM_018177.6:c.3673G= MANE Select	NP_060647.2:p.Ala1225=
NM_001318359.2:c.3433G=	NP_001305288.1:p.Ala1145=