Canonical Allele Identifier: CA439140466

Gene: N4BP2

Linked Data

• MyVariant Identifiers: chr4:g.40123409G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.40121789G>T , CM000666.2:g.40121789G>T	GRCh38
NC_000004.11:g.40123409G>T , CM000666.1:g.40123409G>T	GRCh37
NC_000004.10:g.39799804G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706658.1:c.*3469G>T	ENSP00000516486.1:n.*3469G>T
ENST00000261435.11:c.3678G>T MANE Select	ENSP00000261435.6:p.Val1226=
ENST00000261435.10:c.3678G>T	ENSP00000261435.6:p.Val1226=
ENST00000511480.5:c.*3469G>T	ENSP00000422436.1:n.*3469G>T
ENST00000513269.1:c.2617G>T
NM_018177.4:c.3678G>T	NP_060647.2:p.Val1226=
XM_006714022.2:c.3438G>T	XP_006714085.1:p.Val1146=
XM_006714023.2:c.3438G>T	XP_006714086.1:p.Val1146=
XM_011513715.1:c.4074G>T	XP_011512017.1:p.Val1358=
XM_011513716.1:c.4074G>T	XP_011512018.1:p.Val1358=
XM_011513717.1:c.4074G>T	XP_011512019.1:p.Val1358=
XM_011513718.1:c.3678G>T	XP_011512020.1:p.Val1226=
XM_011513719.1:c.3438G>T	XP_011512021.1:p.Val1146=
XM_011513720.1:c.3438G>T	XP_011512022.1:p.Val1146=
XM_011513721.1:c.3438G>T	XP_011512023.1:p.Val1146=
NM_001318359.1:c.3438G>T	NP_001305288.1:p.Val1146=
NM_018177.5:c.3678G>T	NP_060647.2:p.Val1226=
XM_006714023.3:c.3438G>T	XP_006714086.1:p.Val1146=
XM_011513716.2:c.4074G>T	XP_011512018.1:p.Val1358=
XM_011513717.2:c.4074G>T	XP_011512019.1:p.Val1358=
XM_011513718.2:c.3678G>T	XP_011512020.1:p.Val1226=
XM_011513719.2:c.3438G>T	XP_011512021.1:p.Val1146=
XM_017008397.1:c.4074G>T	XP_016863886.1:p.Val1358=
XM_017008398.1:c.3678G>T	XP_016863887.1:p.Val1226=
XM_017008399.1:c.3438G>T	XP_016863888.1:p.Val1146=
XR_001741283.1:n.4255G>T
NM_018177.6:c.3678G>T MANE Select	NP_060647.2:p.Val1226=
NM_001318359.2:c.3438G>T	NP_001305288.1:p.Val1146=