Canonical Allele Identifier: CA1519891333

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208969G= , CM000666.2:g.186208969G=	GRCh38
NC_000004.11:g.187130123G= , CM000666.1:g.187130123G=	GRCh37
NC_000004.10:g.187367117G=	NCBI36
NG_007965.1:g.22450G=
NG_012095.2:g.4991G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1195G= MANE Select	ENSP00000368079.4:p.Ala399=
ENST00000378802.4:c.1195G=	ENSP00000368079.4:p.Ala399=
ENST00000502665.1:n.430G=
ENST00000507209.5:n.5893G=
ENST00000513354.5:n.285G=
NM_207352.3:c.1195G=	NP_997235.3:p.Ala399=
XM_005262935.2:c.1195G=	XP_005262992.1:p.Ala399=
XM_006714184.2:c.799G=	XP_006714247.1:p.Ala267=
XM_005262935.4:c.1195G=	XP_005262992.1:p.Ala399=
XM_017008037.1:c.799G=	XP_016863526.1:p.Ala267=
NM_207352.4:c.1195G= MANE Select	NP_997235.3:p.Ala399=