Canonical Allele Identifier: CA1519891340

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208977T= , CM000666.2:g.186208977T=	GRCh38
NC_000004.11:g.187130131T= , CM000666.1:g.187130131T=	GRCh37
NC_000004.10:g.187367125T=	NCBI36
NG_007965.1:g.22458T=
NG_012095.2:g.4999T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1203T= MANE Select	ENSP00000368079.4:p.Ser401=
ENST00000378802.4:c.1203T=	ENSP00000368079.4:p.Ser401=
ENST00000502665.1:n.438T=
ENST00000507209.5:n.5901T=
ENST00000513354.5:n.293T=
NM_207352.3:c.1203T=	NP_997235.3:p.Ser401=
XM_005262935.2:c.1203T=	XP_005262992.1:p.Ser401=
XM_006714184.2:c.807T=	XP_006714247.1:p.Ser269=
XM_005262935.4:c.1203T=	XP_005262992.1:p.Ser401=
XM_017008037.1:c.807T=	XP_016863526.1:p.Ser269=
NM_207352.4:c.1203T= MANE Select	NP_997235.3:p.Ser401=