Canonical Allele Identifier: CA1140031031

Gene: CYP4B1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.46813503C= , CM000663.2:g.46813503C=	GRCh38
NC_000001.10:g.47279175C= , CM000663.1:g.47279175C=	GRCh37
NC_000001.9:g.47051762C=	NCBI36
NG_007939.1:g.19506C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001099772.2:c.517C= MANE Select	NP_001093242.1:p.Arg173=
ENST00000371923.9:c.517C= MANE Select	ENSP00000360991.4:p.Arg173=
NM_000779.3:c.517C=	NP_000770.2:p.Arg173=
NM_000779.4:c.517C=	NP_000770.2:p.Arg173=
NM_001099772.1:c.517C=	NP_001093242.1:p.Arg173=
NM_001319161.1:c.472C=	NP_001306090.1:p.Arg158=
NM_001319161.2:c.472C=	NP_001306090.1:p.Arg158=
NM_001319162.1:c.28C=	NP_001306091.1:p.Arg10=
NM_001319162.2:c.28C=	NP_001306091.1:p.Arg10=
NM_001319163.1:c.28C=	NP_001306092.1:p.Arg10=
NM_001319163.2:c.28C=	NP_001306092.1:p.Arg10=
NR_135003.1:n.601C=
NR_135003.2:n.553C=
ENST00000271153.8:c.517C=	ENSP00000271153.4:p.Arg173=
ENST00000371919.8:c.472C=	ENSP00000360987.4:p.Arg158=
ENST00000371923.8:c.517C=	ENSP00000360991.4:p.Arg173=
ENST00000452782.6:n.262C=
ENST00000464439.6:c.517C=	ENSP00000433068.1:p.Arg173=
ENST00000468637.3:n.232C=
ENST00000526297.5:c.28C=	ENSP00000438995.1:p.Arg10=
ENST00000529715.5:c.*227C=	ENSP00000443212.1:n.*227C=
ENST00000534708.6:c.*66C=	ENSP00000433367.2:n.*66C=
ENST00000614163.4:c.517C=	ENSP00000484629.1:p.Arg173=
ENST00000640628.1:c.517C=	ENSP00000492115.1:p.Arg173=
XM_011540831.1:c.472C=	XP_011539133.1:p.Arg158=
XM_011540832.1:c.517C=	XP_011539134.1:p.Arg173=
XM_011540832.2:c.517C=	XP_011539134.1:p.Arg173=
XM_011540833.1:c.-184C=	XP_011539135.1:n.-184C=
XM_011540834.1:c.-181C=	XP_011539136.1:n.-181C=
XM_017000466.1:c.472C=	XP_016855955.1:p.Arg158=
XR_946559.1:n.604C=
XR_946559.2:n.553C=