Canonical Allele Identifier: CA1519920445

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198989T= , CM000666.2:g.186198989T=	GRCh38
NC_000004.11:g.187120143T= , CM000666.1:g.187120143T=	GRCh37
NC_000004.10:g.187357137T=	NCBI36
NG_007965.1:g.12470T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.707T= MANE Select	ENSP00000368079.4:p.Met236=
ENST00000378802.4:c.707T=	ENSP00000368079.4:p.Met236=
ENST00000507209.5:n.1548T=
NM_207352.3:c.707T=	NP_997235.3:p.Met236=
XM_005262935.2:c.707T=	XP_005262992.1:p.Met236=
XM_006714184.2:c.311T=	XP_006714247.1:p.Met104=
XM_005262935.4:c.707T=	XP_005262992.1:p.Met236=
XM_017008037.1:c.311T=	XP_016863526.1:p.Met104=
NM_207352.4:c.707T= MANE Select	NP_997235.3:p.Met236=