Canonical Allele Identifier: CA1519888926

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205198A= , CM000666.2:g.186205198A=	GRCh38
NC_000004.11:g.187126352A= , CM000666.1:g.187126352A=	GRCh37
NC_000004.10:g.187363346A=	NCBI36
NG_007965.1:g.18679A=
NG_012095.2:g.1220A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.988-2A= MANE Select	ENSP00000368079.4:n.988-2A=
ENST00000378802.4:c.988-2A=	ENSP00000368079.4:n.988-2A=
ENST00000502665.1:n.223-2A=
ENST00000507209.5:n.5684A=
ENST00000513354.5:n.78-2A=
NM_207352.3:c.988-2A=	NP_997235.3:n.988-2A=
XM_005262935.2:c.988-2A=	XP_005262992.1:n.988-2A=
XM_006714184.2:c.592-2A=	XP_006714247.1:n.592-2A=
XM_005262935.4:c.988-2A=	XP_005262992.1:n.988-2A=
XM_017008037.1:c.592-2A=	XP_016863526.1:n.592-2A=
NM_207352.4:c.988-2A= MANE Select	NP_997235.3:n.988-2A=