Canonical Allele Identifier: CA1519915053

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194547C= , CM000666.2:g.186194547C=	GRCh38
NC_000004.11:g.187115701C= , CM000666.1:g.187115701C=	GRCh37
NC_000004.10:g.187352695C=	NCBI36
NG_007965.1:g.8028C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.262C= MANE Select	ENSP00000368079.4:p.Pro88=
ENST00000378802.4:c.262C=	ENSP00000368079.4:p.Pro88=
NM_207352.3:c.262C=	NP_997235.3:p.Pro88=
XM_005262935.2:c.262C=	XP_005262992.1:p.Pro88=
XM_006714184.2:c.-49C=	XP_006714247.1:n.-49C=
XM_005262935.4:c.262C=	XP_005262992.1:p.Pro88=
XM_017008037.1:c.-49C=	XP_016863526.1:n.-49C=
NM_207352.4:c.262C= MANE Select	NP_997235.3:p.Pro88=