Canonical Allele Identifier: CA2764867710

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204676_186204677insACT , CM000666.2:g.186204676_186204677insACT	GRCh38
NC_000004.11:g.187125830_187125831insACT , CM000666.1:g.187125830_187125831insACT	GRCh37
NC_000004.10:g.187362824_187362825insACT	NCBI36
NG_007965.1:g.18157_18158insACT
NG_012095.2:g.698_699insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-524_988-523insACT MANE Select	ENSP00000368079.4:n.988-524_988-523insACT
ENST00000378802.4:c.988-524_988-523insACT	ENSP00000368079.4:n.988-524_988-523insACT
ENST00000507209.5:n.5162_5163insACT
ENST00000513354.5:n.77+219_77+220insACT
NM_207352.3:c.988-524_988-523insACT	NP_997235.3:n.988-524_988-523insACT
XM_005262935.2:c.988-524_988-523insACT	XP_005262992.1:n.988-524_988-523insACT
XM_006714184.2:c.592-524_592-523insACT	XP_006714247.1:n.592-524_592-523insACT
XM_005262935.4:c.988-524_988-523insACT	XP_005262992.1:n.988-524_988-523insACT
XM_017008037.1:c.592-524_592-523insACT	XP_016863526.1:n.592-524_592-523insACT
NM_207352.4:c.988-524_988-523insACT MANE Select	NP_997235.3:n.988-524_988-523insACT