Canonical Allele Identifier: CA2764867957

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205332_186205340del , CM000666.2:g.186205332_186205340del	GRCh38
NC_000004.11:g.187126486_187126494del , CM000666.1:g.187126486_187126494del	GRCh37
NC_000004.10:g.187363480_187363488del	NCBI36
NG_007965.1:g.18813_18821del
NG_012095.2:g.1354_1362del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1090+30_1090+38del MANE Select	ENSP00000368079.4:n.1090+30_1090+38del
ENST00000378802.4:c.1090+30_1090+38del	ENSP00000368079.4:n.1090+30_1090+38del
ENST00000502665.1:n.325+30_325+38del
ENST00000507209.5:n.5788+30_5788+38del
ENST00000513354.5:n.180+30_180+38del
NM_207352.3:c.1090+30_1090+38del	NP_997235.3:n.1090+30_1090+38del
XM_005262935.2:c.1090+30_1090+38del	XP_005262992.1:n.1090+30_1090+38del
XM_006714184.2:c.694+30_694+38del	XP_006714247.1:n.694+30_694+38del
XM_005262935.4:c.1090+30_1090+38del	XP_005262992.1:n.1090+30_1090+38del
XM_017008037.1:c.694+30_694+38del	XP_016863526.1:n.694+30_694+38del
NM_207352.4:c.1090+30_1090+38del MANE Select	NP_997235.3:n.1090+30_1090+38del