Canonical Allele Identifier: CA1519888893

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205160A= , CM000666.2:g.186205160A=	GRCh38
NC_000004.11:g.187126314A= , CM000666.1:g.187126314A=	GRCh37
NC_000004.10:g.187363308A=	NCBI36
NG_007965.1:g.18641A=
NG_012095.2:g.1182A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-40A= MANE Select	ENSP00000368079.4:n.988-40A=
ENST00000378802.4:c.988-40A=	ENSP00000368079.4:n.988-40A=
ENST00000502665.1:n.223-40A=
ENST00000507209.5:n.5646A=
ENST00000513354.5:n.78-40A=
NM_207352.3:c.988-40A=	NP_997235.3:n.988-40A=
XM_005262935.2:c.988-40A=	XP_005262992.1:n.988-40A=
XM_006714184.2:c.592-40A=	XP_006714247.1:n.592-40A=
XM_005262935.4:c.988-40A=	XP_005262992.1:n.988-40A=
XM_017008037.1:c.592-40A=	XP_016863526.1:n.592-40A=
NM_207352.4:c.988-40A= MANE Select	NP_997235.3:n.988-40A=