Canonical Allele Identifier: CA2764867725

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204690_186204691insAC , CM000666.2:g.186204690_186204691insAC	GRCh38
NC_000004.11:g.187125844_187125845insAC , CM000666.1:g.187125844_187125845insAC	GRCh37
NC_000004.10:g.187362838_187362839insAC	NCBI36
NG_007965.1:g.18171_18172insAC
NG_012095.2:g.712_713insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-510_988-509insAC MANE Select	ENSP00000368079.4:n.988-510_988-509insAC
ENST00000378802.4:c.988-510_988-509insAC	ENSP00000368079.4:n.988-510_988-509insAC
ENST00000507209.5:n.5176_5177insAC
ENST00000513354.5:n.77+233_77+234insAC
NM_207352.3:c.988-510_988-509insAC	NP_997235.3:n.988-510_988-509insAC
XM_005262935.2:c.988-510_988-509insAC	XP_005262992.1:n.988-510_988-509insAC
XM_006714184.2:c.592-510_592-509insAC	XP_006714247.1:n.592-510_592-509insAC
XM_005262935.4:c.988-510_988-509insAC	XP_005262992.1:n.988-510_988-509insAC
XM_017008037.1:c.592-510_592-509insAC	XP_016863526.1:n.592-510_592-509insAC
NM_207352.4:c.988-510_988-509insAC MANE Select	NP_997235.3:n.988-510_988-509insAC