Canonical Allele Identifier: CA1519891376

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209060C= , CM000666.2:g.186209060C=	GRCh38
NC_000004.11:g.187130214C= , CM000666.1:g.187130214C=	GRCh37
NC_000004.10:g.187367208C=	NCBI36
NG_007965.1:g.22541C=
NG_012095.2:g.5082C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1226-33C= (CYP4V2) MANE Select	ENSP00000368079.4:n.1226-33C=
ENST00000378802.4:c.1226-33C= (CYP4V2)	ENSP00000368079.4:n.1226-33C=
ENST00000502665.1:n.461-33C= (CYP4V2)
ENST00000507209.5:n.5924-33C= (CYP4V2)
ENST00000511608.5:c.22-33C= (KLKB1)
ENST00000513354.5:n.316-33C= (CYP4V2)
NM_207352.3:c.1226-33C= (CYP4V2)	NP_997235.3:n.1226-33C=
XM_005262935.2:c.1226-36C= (CYP4V2)	XP_005262992.1:n.1226-36C=
XM_006714184.2:c.830-33C= (CYP4V2)	XP_006714247.1:n.830-33C=
XM_005262935.4:c.1226-36C= (CYP4V2)	XP_005262992.1:n.1226-36C=
XM_017008037.1:c.830-33C= (CYP4V2)	XP_016863526.1:n.830-33C=
NM_207352.4:c.1226-33C= (CYP4V2) MANE Select	NP_997235.3:n.1226-33C=