Canonical Allele Identifier: CA2764867685

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204663_186204664insC , CM000666.2:g.186204663_186204664insC	GRCh38
NC_000004.11:g.187125817_187125818insC , CM000666.1:g.187125817_187125818insC	GRCh37
NC_000004.10:g.187362811_187362812insC	NCBI36
NG_007965.1:g.18144_18145insC
NG_012095.2:g.685_686insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-537_988-536insC MANE Select	ENSP00000368079.4:n.988-537_988-536insC
ENST00000378802.4:c.988-537_988-536insC	ENSP00000368079.4:n.988-537_988-536insC
ENST00000507209.5:n.5149_5150insC
ENST00000513354.5:n.77+206_77+207insC
NM_207352.3:c.988-537_988-536insC	NP_997235.3:n.988-537_988-536insC
XM_005262935.2:c.988-537_988-536insC	XP_005262992.1:n.988-537_988-536insC
XM_006714184.2:c.592-537_592-536insC	XP_006714247.1:n.592-537_592-536insC
XM_005262935.4:c.988-537_988-536insC	XP_005262992.1:n.988-537_988-536insC
XM_017008037.1:c.592-537_592-536insC	XP_016863526.1:n.592-537_592-536insC
NM_207352.4:c.988-537_988-536insC MANE Select	NP_997235.3:n.988-537_988-536insC