Canonical Allele Identifier: CA2764867795

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204728_186204729insC , CM000666.2:g.186204728_186204729insC	GRCh38
NC_000004.11:g.187125882_187125883insC , CM000666.1:g.187125882_187125883insC	GRCh37
NC_000004.10:g.187362876_187362877insC	NCBI36
NG_007965.1:g.18209_18210insC
NG_012095.2:g.750_751insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-472_988-471insC MANE Select	ENSP00000368079.4:n.988-472_988-471insC
ENST00000378802.4:c.988-472_988-471insC	ENSP00000368079.4:n.988-472_988-471insC
ENST00000507209.5:n.5214_5215insC
ENST00000513354.5:n.77+271_77+272insC
NM_207352.3:c.988-472_988-471insC	NP_997235.3:n.988-472_988-471insC
XM_005262935.2:c.988-472_988-471insC	XP_005262992.1:n.988-472_988-471insC
XM_006714184.2:c.592-472_592-471insC	XP_006714247.1:n.592-472_592-471insC
XM_005262935.4:c.988-472_988-471insC	XP_005262992.1:n.988-472_988-471insC
XM_017008037.1:c.592-472_592-471insC	XP_016863526.1:n.592-472_592-471insC
NM_207352.4:c.988-472_988-471insC MANE Select	NP_997235.3:n.988-472_988-471insC