Canonical Allele Identifier: CA1519888613

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204887_186204889delinsCTT , CM000666.2:g.186204887_186204889delinsCTT	GRCh38
NC_000004.11:g.187126041_187126043delinsCTT , CM000666.1:g.187126041_187126043delinsCTT	GRCh37
NC_000004.10:g.187363035_187363037delinsCTT	NCBI36
NG_007965.1:g.18368_18370delinsCTT
NG_012095.2:g.909_911delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-313_988-311delinsCTT MANE Select	ENSP00000368079.4:n.988-313_988-311delinsCTT
ENST00000378802.4:c.988-313_988-311delinsCTT	ENSP00000368079.4:n.988-313_988-311delinsCTT
ENST00000502665.1:n.51_53delinsCTT
ENST00000507209.5:n.5373_5375delinsCTT
ENST00000513354.5:n.78-313_78-311delinsCTT
NM_207352.3:c.988-313_988-311delinsCTT	NP_997235.3:n.988-313_988-311delinsCTT
XM_005262935.2:c.988-313_988-311delinsCTT	XP_005262992.1:n.988-313_988-311delinsCTT
XM_006714184.2:c.592-313_592-311delinsCTT	XP_006714247.1:n.592-313_592-311delinsCTT
XM_005262935.4:c.988-313_988-311delinsCTT	XP_005262992.1:n.988-313_988-311delinsCTT
XM_017008037.1:c.592-313_592-311delinsCTT	XP_016863526.1:n.592-313_592-311delinsCTT
NM_207352.4:c.988-313_988-311delinsCTT MANE Select	NP_997235.3:n.988-313_988-311delinsCTT