Canonical Allele Identifier: CA1519891502

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209267G= , CM000666.2:g.186209267G=	GRCh38
NC_000004.11:g.187130421G= , CM000666.1:g.187130421G=	GRCh37
NC_000004.10:g.187367415G=	NCBI36
NG_007965.1:g.22748G=
NG_012095.2:g.5289G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1400G= MANE Select	ENSP00000368079.4:p.Cys467=
ENST00000378802.4:c.1400G=	ENSP00000368079.4:p.Cys467=
ENST00000502665.1:n.635G=
ENST00000507209.5:n.6098G=
ENST00000511608.5:n.196G=
ENST00000513354.5:n.490G=
NM_207352.3:c.1400G=	NP_997235.3:p.Cys467=
XM_005262935.2:c.1397G=	XP_005262992.1:p.Cys466=
XM_006714184.2:c.1004G=	XP_006714247.1:p.Cys335=
XM_005262935.4:c.1397G=	XP_005262992.1:p.Cys466=
XM_017008037.1:c.1004G=	XP_016863526.1:p.Cys335=
NM_207352.4:c.1400G= MANE Select	NP_997235.3:p.Cys467=