Canonical Allele Identifier: CA1519915222

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194606T= , CM000666.2:g.186194606T=	GRCh38
NC_000004.11:g.187115760T= , CM000666.1:g.187115760T=	GRCh37
NC_000004.10:g.187352754T=	NCBI36
NG_007965.1:g.8087T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.321T= MANE Select	ENSP00000368079.4:p.Asn107=
ENST00000378802.4:c.321T=	ENSP00000368079.4:p.Asn107=
NM_207352.3:c.321T=	NP_997235.3:p.Asn107=
XM_005262935.2:c.321T=	XP_005262992.1:p.Asn107=
XM_006714184.2:c.11T=	XP_006714247.1:p.Met4=
XM_005262935.4:c.321T=	XP_005262992.1:p.Asn107=
XM_017008037.1:c.11T=	XP_016863526.1:p.Met4=
NM_207352.4:c.321T= MANE Select	NP_997235.3:p.Asn107=