Canonical Allele Identifier: CA1519918616

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197087C= , CM000666.2:g.186197087C=	GRCh38
NC_000004.11:g.187118241C= , CM000666.1:g.187118241C=	GRCh37
NC_000004.10:g.187355235C=	NCBI36
NG_007965.1:g.10568C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.561C= MANE Select	ENSP00000368079.4:p.Asn187=
ENST00000378802.4:c.561C=	ENSP00000368079.4:p.Asn187=
ENST00000507209.5:n.1000C=
NM_207352.3:c.561C=	NP_997235.3:p.Asn187=
XM_005262935.2:c.561C=	XP_005262992.1:p.Asn187=
XM_006714184.2:c.165C=	XP_006714247.1:p.Asn55=
XM_005262935.4:c.561C=	XP_005262992.1:p.Asn187=
XM_017008037.1:c.165C=	XP_016863526.1:p.Asn55=
NM_207352.4:c.561C= MANE Select	NP_997235.3:p.Asn187=