Canonical Allele Identifier: CA2764868920

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209370_186209371insAC , CM000666.2:g.186209370_186209371insAC	GRCh38
NC_000004.11:g.187130524_187130525insAC , CM000666.1:g.187130524_187130525insAC	GRCh37
NC_000004.10:g.187367518_187367519insAC	NCBI36
NG_007965.1:g.22851_22852insAC
NG_012095.2:g.5392_5393insAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1405+98_1405+99insAC (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+98_1405+99insAC
ENST00000378802.4:c.1405+98_1405+99insAC (CYP4V2)	ENSP00000368079.4:n.1405+98_1405+99insAC
ENST00000502665.1:n.640+98_640+99insAC (CYP4V2)
ENST00000507209.5:n.6103+98_6103+99insAC (CYP4V2)
ENST00000511608.5:c.201+98_201+99insAC (KLKB1)
ENST00000513354.5:n.495+98_495+99insAC (CYP4V2)
NM_207352.3:c.1405+98_1405+99insAC (CYP4V2)	NP_997235.3:n.1405+98_1405+99insAC
XM_005262935.2:c.1402+98_1402+99insAC (CYP4V2)	XP_005262992.1:n.1402+98_1402+99insAC
XM_006714184.2:c.1009+98_1009+99insAC (CYP4V2)	XP_006714247.1:n.1009+98_1009+99insAC
XM_005262935.4:c.1402+98_1402+99insAC (CYP4V2)	XP_005262992.1:n.1402+98_1402+99insAC
XM_017008037.1:c.1009+98_1009+99insAC (CYP4V2)	XP_016863526.1:n.1009+98_1009+99insAC
NM_207352.4:c.1405+98_1405+99insAC (CYP4V2) MANE Select	NP_997235.3:n.1405+98_1405+99insAC