Canonical Allele Identifier: CA1519888652

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204932C= , CM000666.2:g.186204932C=	GRCh38
NC_000004.11:g.187126086C= , CM000666.1:g.187126086C=	GRCh37
NC_000004.10:g.187363080C=	NCBI36
NG_007965.1:g.18413C=
NG_012095.2:g.954C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-268C= MANE Select	ENSP00000368079.4:n.988-268C=
ENST00000378802.4:c.988-268C=	ENSP00000368079.4:n.988-268C=
ENST00000502665.1:n.96C=
ENST00000507209.5:n.5418C=
ENST00000513354.5:n.78-268C=
NM_207352.3:c.988-268C=	NP_997235.3:n.988-268C=
XM_005262935.2:c.988-268C=	XP_005262992.1:n.988-268C=
XM_006714184.2:c.592-268C=	XP_006714247.1:n.592-268C=
XM_005262935.4:c.988-268C=	XP_005262992.1:n.988-268C=
XM_017008037.1:c.592-268C=	XP_016863526.1:n.592-268C=
NM_207352.4:c.988-268C= MANE Select	NP_997235.3:n.988-268C=