Canonical Allele Identifier: CA2764867280

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194717_186194718insC , CM000666.2:g.186194717_186194718insC	GRCh38
NC_000004.11:g.187115871_187115872insC , CM000666.1:g.187115871_187115872insC	GRCh37
NC_000004.10:g.187352865_187352866insC	NCBI36
NG_007965.1:g.8198_8199insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.327+105_327+106insC MANE Select	ENSP00000368079.4:n.327+105_327+106insC
ENST00000378802.4:c.327+105_327+106insC	ENSP00000368079.4:n.327+105_327+106insC
NM_207352.3:c.327+105_327+106insC	NP_997235.3:n.327+105_327+106insC
XM_005262935.2:c.327+105_327+106insC	XP_005262992.1:n.327+105_327+106insC
XM_006714184.2:c.17+105_17+106insC	XP_006714247.1:n.17+105_17+106insC
XM_005262935.4:c.327+105_327+106insC	XP_005262992.1:n.327+105_327+106insC
XM_017008037.1:c.17+105_17+106insC	XP_016863526.1:n.17+105_17+106insC
NM_207352.4:c.327+105_327+106insC MANE Select	NP_997235.3:n.327+105_327+106insC