Canonical Allele Identifier: CA2764867889

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204866_186204869del , CM000666.2:g.186204866_186204869del	GRCh38
NC_000004.11:g.187126020_187126023del , CM000666.1:g.187126020_187126023del	GRCh37
NC_000004.10:g.187363014_187363017del	NCBI36
NG_007965.1:g.18347_18350del
NG_012095.2:g.888_891del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-334_988-331del MANE Select	ENSP00000368079.4:n.988-334_988-331del
ENST00000378802.4:c.988-334_988-331del	ENSP00000368079.4:n.988-334_988-331del
ENST00000502665.1:n.30_33del
ENST00000507209.5:n.5352_5355del
ENST00000513354.5:n.78-334_78-331del
NM_207352.3:c.988-334_988-331del	NP_997235.3:n.988-334_988-331del
XM_005262935.2:c.988-334_988-331del	XP_005262992.1:n.988-334_988-331del
XM_006714184.2:c.592-334_592-331del	XP_006714247.1:n.592-334_592-331del
XM_005262935.4:c.988-334_988-331del	XP_005262992.1:n.988-334_988-331del
XM_017008037.1:c.592-334_592-331del	XP_016863526.1:n.592-334_592-331del
NM_207352.4:c.988-334_988-331del MANE Select	NP_997235.3:n.988-334_988-331del