Canonical Allele Identifier: CA1519888502

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204792C= , CM000666.2:g.186204792C=	GRCh38
NC_000004.11:g.187125946C= , CM000666.1:g.187125946C=	GRCh37
NC_000004.10:g.187362940C=	NCBI36
NG_007965.1:g.18273C=
NG_012095.2:g.814C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-408C= MANE Select	ENSP00000368079.4:n.988-408C=
ENST00000378802.4:c.988-408C=	ENSP00000368079.4:n.988-408C=
ENST00000507209.5:n.5278C=
ENST00000513354.5:n.77+335C=
NM_207352.3:c.988-408C=	NP_997235.3:n.988-408C=
XM_005262935.2:c.988-408C=	XP_005262992.1:n.988-408C=
XM_006714184.2:c.592-408C=	XP_006714247.1:n.592-408C=
XM_005262935.4:c.988-408C=	XP_005262992.1:n.988-408C=
XM_017008037.1:c.592-408C=	XP_016863526.1:n.592-408C=
NM_207352.4:c.988-408C= MANE Select	NP_997235.3:n.988-408C=