Canonical Allele Identifier: CA1519910901

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186191924T= , CM000666.2:g.186191924T=	GRCh38
NC_000004.11:g.187113078T= , CM000666.1:g.187113078T=	GRCh37
NC_000004.10:g.187350072T=	NCBI36
NG_007965.1:g.5405T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.101T= MANE Select	ENSP00000368079.4:p.Leu34=
ENST00000378802.4:c.101T=	ENSP00000368079.4:p.Leu34=
NM_207352.3:c.101T=	NP_997235.3:p.Leu34=
XM_005262935.2:c.101T=	XP_005262992.1:p.Leu34=
XM_005262935.4:c.101T=	XP_005262992.1:p.Leu34=
XM_017008037.1:c.-210T=	XP_016863526.1:n.-210T=
NM_207352.4:c.101T= MANE Select	NP_997235.3:p.Leu34=