Canonical Allele Identifier: CA1519892521

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211457G= , CM000666.2:g.186211457G=	GRCh38
NC_000004.11:g.187132611G= , CM000666.1:g.187132611G=	GRCh37
NC_000004.10:g.187369605G=	NCBI36
NG_007965.1:g.24938G=
NG_012095.2:g.7479G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*816G= (CYP4V2) MANE Select	ENSP00000368079.4:n.*816G=
ENST00000502665.1:n.1629G= (CYP4V2)
ENST00000507209.5:n.7092G= (CYP4V2)
ENST00000511608.5:c.201+2185G= (KLKB1)
NM_207352.3:c.*816G= (CYP4V2)	NP_997235.3:n.*816G=
XM_005262935.2:c.*816G= (CYP4V2)	XP_005262992.1:n.*816G=
XM_006714184.2:c.*816G= (CYP4V2)	XP_006714247.1:n.*816G=
XM_011531931.1:c.-3252G= (KLKB1)	XP_011530233.1:n.-3252G=
XM_011531932.1:c.-3502G= (KLKB1)	XP_011530234.1:n.-3502G=
XM_011531933.1:c.-3316G= (KLKB1)	XP_011530235.1:n.-3316G=
XM_005262935.4:c.*816G= (CYP4V2)	XP_005262992.1:n.*816G=
XM_017008037.1:c.*816G= (CYP4V2)	XP_016863526.1:n.*816G=
NM_207352.4:c.*816G= (CYP4V2) MANE Select	NP_997235.3:n.*816G=