Canonical Allele Identifier: CA1519919428

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197602G= , CM000666.2:g.186197602G=	GRCh38
NC_000004.11:g.187118756G= , CM000666.1:g.187118756G=	GRCh37
NC_000004.10:g.187355750G=	NCBI36
NG_007965.1:g.11083G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674G= MANE Select	ENSP00000368079.4:p.Arg225=
ENST00000378802.4:c.674G=	ENSP00000368079.4:p.Arg225=
ENST00000507209.5:n.1515G=
NM_207352.3:c.674G=	NP_997235.3:p.Arg225=
XM_005262935.2:c.674G=	XP_005262992.1:p.Arg225=
XM_006714184.2:c.278G=	XP_006714247.1:p.Arg93=
XM_005262935.4:c.674G=	XP_005262992.1:p.Arg225=
XM_017008037.1:c.278G=	XP_016863526.1:p.Arg93=
NM_207352.4:c.674G= MANE Select	NP_997235.3:p.Arg225=