Canonical Allele Identifier: CA1519891181

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208688T= , CM000666.2:g.186208688T=	GRCh38
NC_000004.11:g.187129842T= , CM000666.1:g.187129842T=	GRCh37
NC_000004.10:g.187366836T=	NCBI36
NG_007965.1:g.22169T=
NG_012095.2:g.4710T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-177T= MANE Select	ENSP00000368079.4:n.1091-177T=
ENST00000378802.4:c.1091-177T=	ENSP00000368079.4:n.1091-177T=
ENST00000502665.1:n.326-177T=
ENST00000507209.5:n.5789-177T=
ENST00000513354.5:n.181-177T=
NM_207352.3:c.1091-177T=	NP_997235.3:n.1091-177T=
XM_005262935.2:c.1091-177T=	XP_005262992.1:n.1091-177T=
XM_006714184.2:c.695-177T=	XP_006714247.1:n.695-177T=
XM_005262935.4:c.1091-177T=	XP_005262992.1:n.1091-177T=
XM_017008037.1:c.695-177T=	XP_016863526.1:n.695-177T=
NM_207352.4:c.1091-177T= MANE Select	NP_997235.3:n.1091-177T=