Canonical Allele Identifier: CA1519918285

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186196951A= , CM000666.2:g.186196951A=	GRCh38
NC_000004.11:g.187118105A= , CM000666.1:g.187118105A=	GRCh37
NC_000004.10:g.187355099A=	NCBI36
NG_007965.1:g.10432A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.425A= MANE Select	ENSP00000368079.4:p.Lys142=
ENST00000378802.4:c.425A=	ENSP00000368079.4:p.Lys142=
ENST00000507209.5:n.864A=
NM_207352.3:c.425A=	NP_997235.3:p.Lys142=
XM_005262935.2:c.425A=	XP_005262992.1:p.Lys142=
XM_006714184.2:c.29A=	XP_006714247.1:p.Lys10=
XM_005262935.4:c.425A=	XP_005262992.1:p.Lys142=
XM_017008037.1:c.29A=	XP_016863526.1:p.Lys10=
NM_207352.4:c.425A= MANE Select	NP_997235.3:p.Lys142=