Canonical Allele Identifier: CA1519889482

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205677C= , CM000666.2:g.186205677C=	GRCh38
NC_000004.11:g.187126831C= , CM000666.1:g.187126831C=	GRCh37
NC_000004.10:g.187363825C=	NCBI36
NG_007965.1:g.19158C=
NG_012095.2:g.1699C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+375C= MANE Select	ENSP00000368079.4:n.1090+375C=
ENST00000378802.4:c.1090+375C=	ENSP00000368079.4:n.1090+375C=
ENST00000502665.1:n.325+375C=
ENST00000507209.5:n.5788+375C=
ENST00000513354.5:n.180+375C=
NM_207352.3:c.1090+375C=	NP_997235.3:n.1090+375C=
XM_005262935.2:c.1090+375C=	XP_005262992.1:n.1090+375C=
XM_006714184.2:c.694+375C=	XP_006714247.1:n.694+375C=
XM_005262935.4:c.1090+375C=	XP_005262992.1:n.1090+375C=
XM_017008037.1:c.694+375C=	XP_016863526.1:n.694+375C=
NM_207352.4:c.1090+375C= MANE Select	NP_997235.3:n.1090+375C=