Canonical Allele Identifier: CA1519920477

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186199084G= , CM000666.2:g.186199084G=	GRCh38
NC_000004.11:g.187120238G= , CM000666.1:g.187120238G=	GRCh37
NC_000004.10:g.187357232G=	NCBI36
NG_007965.1:g.12565G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.801+1G= MANE Select	ENSP00000368079.4:n.801+1G=
ENST00000378802.4:c.801+1G=	ENSP00000368079.4:n.801+1G=
ENST00000507209.5:n.1642+1G=
NM_207352.3:c.801+1G=	NP_997235.3:n.801+1G=
XM_005262935.2:c.801+1G=	XP_005262992.1:n.801+1G=
XM_006714184.2:c.405+1G=	XP_006714247.1:n.405+1G=
XM_005262935.4:c.801+1G=	XP_005262992.1:n.801+1G=
XM_017008037.1:c.405+1G=	XP_016863526.1:n.405+1G=
NM_207352.4:c.801+1G= MANE Select	NP_997235.3:n.801+1G=