Canonical Allele Identifier: CA1519892418

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211210A= , CM000666.2:g.186211210A=	GRCh38
NC_000004.11:g.187132364A= , CM000666.1:g.187132364A=	GRCh37
NC_000004.10:g.187369358A=	NCBI36
NG_007965.1:g.24691A=
NG_012095.2:g.7232A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*569A= (CYP4V2) MANE Select	ENSP00000368079.4:n.*569A=
ENST00000502665.1:n.1382A= (CYP4V2)
ENST00000507209.5:n.6845A= (CYP4V2)
ENST00000511608.5:c.201+1938A= (KLKB1)
NM_207352.3:c.*569A= (CYP4V2)	NP_997235.3:n.*569A=
XM_005262935.2:c.*569A= (CYP4V2)	XP_005262992.1:n.*569A=
XM_006714184.2:c.*569A= (CYP4V2)	XP_006714247.1:n.*569A=
XM_011531931.1:c.-3499A= (KLKB1)	XP_011530233.1:n.-3499A=
XM_011531932.1:c.-3749A= (KLKB1)	XP_011530234.1:n.-3749A=
XM_011531933.1:c.-3563A= (KLKB1)	XP_011530235.1:n.-3563A=
XM_005262935.4:c.*569A= (CYP4V2)	XP_005262992.1:n.*569A=
XM_017008037.1:c.*569A= (CYP4V2)	XP_016863526.1:n.*569A=
NM_207352.4:c.*569A= (CYP4V2) MANE Select	NP_997235.3:n.*569A=