Canonical Allele Identifier: CA1519883851

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200634G= , CM000666.2:g.186200634G=	GRCh38
NC_000004.11:g.187121788G= , CM000666.1:g.187121788G=	GRCh37
NC_000004.10:g.187358782G=	NCBI36
NG_007965.1:g.14115G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-523G= MANE Select	ENSP00000368079.4:n.802-523G=
ENST00000378802.4:c.802-523G=	ENSP00000368079.4:n.802-523G=
ENST00000507209.5:n.1643-523G=
NM_207352.3:c.802-523G=	NP_997235.3:n.802-523G=
XM_005262935.2:c.802-523G=	XP_005262992.1:n.802-523G=
XM_006714184.2:c.406-523G=	XP_006714247.1:n.406-523G=
XM_005262935.4:c.802-523G=	XP_005262992.1:n.802-523G=
XM_017008037.1:c.406-523G=	XP_016863526.1:n.406-523G=
NM_207352.4:c.802-523G= MANE Select	NP_997235.3:n.802-523G=