Canonical Allele Identifier: CA1519888515

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204796_186204797delinsCT , CM000666.2:g.186204796_186204797delinsCT	GRCh38
NC_000004.11:g.187125950_187125951delinsCT , CM000666.1:g.187125950_187125951delinsCT	GRCh37
NC_000004.10:g.187362944_187362945delinsCT	NCBI36
NG_007965.1:g.18277_18278delinsCT
NG_012095.2:g.818_819delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-404_988-403delinsCT MANE Select	ENSP00000368079.4:n.988-404_988-403delinsCT
ENST00000378802.4:c.988-404_988-403delinsCT	ENSP00000368079.4:n.988-404_988-403delinsCT
ENST00000507209.5:n.5282_5283delinsCT
ENST00000513354.5:n.77+339_77+340delinsCT
NM_207352.3:c.988-404_988-403delinsCT	NP_997235.3:n.988-404_988-403delinsCT
XM_005262935.2:c.988-404_988-403delinsCT	XP_005262992.1:n.988-404_988-403delinsCT
XM_006714184.2:c.592-404_592-403delinsCT	XP_006714247.1:n.592-404_592-403delinsCT
XM_005262935.4:c.988-404_988-403delinsCT	XP_005262992.1:n.988-404_988-403delinsCT
XM_017008037.1:c.592-404_592-403delinsCT	XP_016863526.1:n.592-404_592-403delinsCT
NM_207352.4:c.988-404_988-403delinsCT MANE Select	NP_997235.3:n.988-404_988-403delinsCT