Canonical Allele Identifier: CA1519918636

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197095T= , CM000666.2:g.186197095T=	GRCh38
NC_000004.11:g.187118249T= , CM000666.1:g.187118249T=	GRCh37
NC_000004.10:g.187355243T=	NCBI36
NG_007965.1:g.10576T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.569T= MANE Select	ENSP00000368079.4:p.Phe190=
ENST00000378802.4:c.569T=	ENSP00000368079.4:p.Phe190=
ENST00000507209.5:n.1008T=
NM_207352.3:c.569T=	NP_997235.3:p.Phe190=
XM_005262935.2:c.569T=	XP_005262992.1:p.Phe190=
XM_006714184.2:c.173T=	XP_006714247.1:p.Phe58=
XM_005262935.4:c.569T=	XP_005262992.1:p.Phe190=
XM_017008037.1:c.173T=	XP_016863526.1:p.Phe58=
NM_207352.4:c.569T= MANE Select	NP_997235.3:p.Phe190=