Canonical Allele Identifier: CA1519888575

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204851_186204855delinsAGTAC , CM000666.2:g.186204851_186204855delinsAGTAC	GRCh38
NC_000004.11:g.187126005_187126009delinsAGTAC , CM000666.1:g.187126005_187126009delinsAGTAC	GRCh37
NC_000004.10:g.187362999_187363003delinsAGTAC	NCBI36
NG_007965.1:g.18332_18336delinsAGTAC
NG_012095.2:g.873_877delinsAGTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-349_988-345delinsAGTAC MANE Select	ENSP00000368079.4:n.988-349_988-345delinsAGTAC
ENST00000378802.4:c.988-349_988-345delinsAGTAC	ENSP00000368079.4:n.988-349_988-345delinsAGTAC
ENST00000502665.1:n.15_19delinsAGTAC
ENST00000507209.5:n.5337_5341delinsAGTAC
ENST00000513354.5:n.78-349_78-345delinsAGTAC
NM_207352.3:c.988-349_988-345delinsAGTAC	NP_997235.3:n.988-349_988-345delinsAGTAC
XM_005262935.2:c.988-349_988-345delinsAGTAC	XP_005262992.1:n.988-349_988-345delinsAGTAC
XM_006714184.2:c.592-349_592-345delinsAGTAC	XP_006714247.1:n.592-349_592-345delinsAGTAC
XM_005262935.4:c.988-349_988-345delinsAGTAC	XP_005262992.1:n.988-349_988-345delinsAGTAC
XM_017008037.1:c.592-349_592-345delinsAGTAC	XP_016863526.1:n.592-349_592-345delinsAGTAC
NM_207352.4:c.988-349_988-345delinsAGTAC MANE Select	NP_997235.3:n.988-349_988-345delinsAGTAC