Canonical Allele Identifier: CA1519892613

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211652G= , CM000666.2:g.186211652G=	GRCh38
NC_000004.11:g.187132806G= , CM000666.1:g.187132806G=	GRCh37
NC_000004.10:g.187369800G=	NCBI36
NG_007965.1:g.25133G=
NG_012095.2:g.7674G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*1011G= (CYP4V2) MANE Select	ENSP00000368079.4:n.*1011G=
ENST00000502665.1:n.1824G= (CYP4V2)
ENST00000507209.5:n.7287G= (CYP4V2)
ENST00000511608.5:c.201+2380G= (KLKB1)
NM_207352.3:c.*1011G= (CYP4V2)	NP_997235.3:n.*1011G=
XM_005262935.2:c.*1011G= (CYP4V2)	XP_005262992.1:n.*1011G=
XM_006714184.2:c.*1011G= (CYP4V2)	XP_006714247.1:n.*1011G=
XM_011531931.1:c.-3057G= (KLKB1)	XP_011530233.1:n.-3057G=
XM_011531932.1:c.-3307G= (KLKB1)	XP_011530234.1:n.-3307G=
XM_011531933.1:c.-3121G= (KLKB1)	XP_011530235.1:n.-3121G=
XM_005262935.4:c.*1011G= (CYP4V2)	XP_005262992.1:n.*1011G=
XM_017008037.1:c.*1011G= (CYP4V2)	XP_016863526.1:n.*1011G=
NM_207352.4:c.*1011G= (CYP4V2) MANE Select	NP_997235.3:n.*1011G=