Canonical Allele Identifier: CA1519892536

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211476G= , CM000666.2:g.186211476G=	GRCh38
NC_000004.11:g.187132630G= , CM000666.1:g.187132630G=	GRCh37
NC_000004.10:g.187369624G=	NCBI36
NG_007965.1:g.24957G=
NG_012095.2:g.7498G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*835G= (CYP4V2) MANE Select	ENSP00000368079.4:n.*835G=
ENST00000502665.1:n.1648G= (CYP4V2)
ENST00000507209.5:n.7111G= (CYP4V2)
ENST00000511608.5:c.201+2204G= (KLKB1)
NM_207352.3:c.*835G= (CYP4V2)	NP_997235.3:n.*835G=
XM_005262935.2:c.*835G= (CYP4V2)	XP_005262992.1:n.*835G=
XM_006714184.2:c.*835G= (CYP4V2)	XP_006714247.1:n.*835G=
XM_011531931.1:c.-3233G= (KLKB1)	XP_011530233.1:n.-3233G=
XM_011531932.1:c.-3483G= (KLKB1)	XP_011530234.1:n.-3483G=
XM_011531933.1:c.-3297G= (KLKB1)	XP_011530235.1:n.-3297G=
XM_005262935.4:c.*835G= (CYP4V2)	XP_005262992.1:n.*835G=
XM_017008037.1:c.*835G= (CYP4V2)	XP_016863526.1:n.*835G=
NM_207352.4:c.*835G= (CYP4V2) MANE Select	NP_997235.3:n.*835G=