Canonical Allele Identifier: CA1519919343

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197554T= , CM000666.2:g.186197554T=	GRCh38
NC_000004.11:g.187118708T= , CM000666.1:g.187118708T=	GRCh37
NC_000004.10:g.187355702T=	NCBI36
NG_007965.1:g.11035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.626T= MANE Select	ENSP00000368079.4:p.Ile209=
ENST00000378802.4:c.626T=	ENSP00000368079.4:p.Ile209=
ENST00000507209.5:n.1467T=
NM_207352.3:c.626T=	NP_997235.3:p.Ile209=
XM_005262935.2:c.626T=	XP_005262992.1:p.Ile209=
XM_006714184.2:c.230T=	XP_006714247.1:p.Ile77=
XM_005262935.4:c.626T=	XP_005262992.1:p.Ile209=
XM_017008037.1:c.230T=	XP_016863526.1:p.Ile77=
NM_207352.4:c.626T= MANE Select	NP_997235.3:p.Ile209=