Canonical Allele Identifier: CA1519889488

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205683A= , CM000666.2:g.186205683A=	GRCh38
NC_000004.11:g.187126837A= , CM000666.1:g.187126837A=	GRCh37
NC_000004.10:g.187363831A=	NCBI36
NG_007965.1:g.19164A=
NG_012095.2:g.1705A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+381A= MANE Select	ENSP00000368079.4:n.1090+381A=
ENST00000378802.4:c.1090+381A=	ENSP00000368079.4:n.1090+381A=
ENST00000502665.1:n.325+381A=
ENST00000507209.5:n.5788+381A=
ENST00000513354.5:n.180+381A=
NM_207352.3:c.1090+381A=	NP_997235.3:n.1090+381A=
XM_005262935.2:c.1090+381A=	XP_005262992.1:n.1090+381A=
XM_006714184.2:c.694+381A=	XP_006714247.1:n.694+381A=
XM_005262935.4:c.1090+381A=	XP_005262992.1:n.1090+381A=
XM_017008037.1:c.694+381A=	XP_016863526.1:n.694+381A=
NM_207352.4:c.1090+381A= MANE Select	NP_997235.3:n.1090+381A=