Canonical Allele Identifier: CA1519920464

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199048_186199050delinsAAG , CM000666.2:g.186199048_186199050delinsAAG	GRCh38
NC_000004.11:g.187120202_187120204delinsAAG , CM000666.1:g.187120202_187120204delinsAAG	GRCh37
NC_000004.10:g.187357196_187357198delinsAAG	NCBI36
NG_007965.1:g.12529_12531delinsAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.766_768delinsAAG MANE Select	ENSP00000368079.4:p.Lys256=
ENST00000378802.4:c.766_768delinsAAG	ENSP00000368079.4:p.Lys256=
ENST00000507209.5:n.1607_1609delinsAAG
NM_207352.3:c.766_768delinsAAG	NP_997235.3:p.Lys256=
XM_005262935.2:c.766_768delinsAAG	XP_005262992.1:p.Lys256=
XM_006714184.2:c.370_372delinsAAG	XP_006714247.1:p.Lys124=
XM_005262935.4:c.766_768delinsAAG	XP_005262992.1:p.Lys256=
XM_017008037.1:c.370_372delinsAAG	XP_016863526.1:p.Lys124=
NM_207352.4:c.766_768delinsAAG MANE Select	NP_997235.3:p.Lys256=