Canonical Allele Identifier: CA1519891526

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209331C= , CM000666.2:g.186209331C=	GRCh38
NC_000004.11:g.187130485C= , CM000666.1:g.187130485C=	GRCh37
NC_000004.10:g.187367479C=	NCBI36
NG_007965.1:g.22812C=
NG_012095.2:g.5353C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1405+59C= (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+59C=
ENST00000378802.4:c.1405+59C= (CYP4V2)	ENSP00000368079.4:n.1405+59C=
ENST00000502665.1:n.640+59C= (CYP4V2)
ENST00000507209.5:n.6103+59C= (CYP4V2)
ENST00000511608.5:c.201+59C= (KLKB1)
ENST00000513354.5:n.495+59C= (CYP4V2)
NM_207352.3:c.1405+59C= (CYP4V2)	NP_997235.3:n.1405+59C=
XM_005262935.2:c.1402+59C= (CYP4V2)	XP_005262992.1:n.1402+59C=
XM_006714184.2:c.1009+59C= (CYP4V2)	XP_006714247.1:n.1009+59C=
XM_005262935.4:c.1402+59C= (CYP4V2)	XP_005262992.1:n.1402+59C=
XM_017008037.1:c.1009+59C= (CYP4V2)	XP_016863526.1:n.1009+59C=
NM_207352.4:c.1405+59C= (CYP4V2) MANE Select	NP_997235.3:n.1405+59C=