Canonical Allele Identifier: CA2764868926

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209377_186209378insA , CM000666.2:g.186209377_186209378insA	GRCh38
NC_000004.11:g.187130531_187130532insA , CM000666.1:g.187130531_187130532insA	GRCh37
NC_000004.10:g.187367525_187367526insA	NCBI36
NG_007965.1:g.22858_22859insA
NG_012095.2:g.5399_5400insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1405+105_1405+106insA (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+105_1405+106insA
ENST00000378802.4:c.1405+105_1405+106insA (CYP4V2)	ENSP00000368079.4:n.1405+105_1405+106insA
ENST00000502665.1:n.640+105_640+106insA (CYP4V2)
ENST00000507209.5:n.6103+105_6103+106insA (CYP4V2)
ENST00000511608.5:c.201+105_201+106insA (KLKB1)
ENST00000513354.5:n.495+105_495+106insA (CYP4V2)
NM_207352.3:c.1405+105_1405+106insA (CYP4V2)	NP_997235.3:n.1405+105_1405+106insA
XM_005262935.2:c.1402+105_1402+106insA (CYP4V2)	XP_005262992.1:n.1402+105_1402+106insA
XM_006714184.2:c.1009+105_1009+106insA (CYP4V2)	XP_006714247.1:n.1009+105_1009+106insA
XM_005262935.4:c.1402+105_1402+106insA (CYP4V2)	XP_005262992.1:n.1402+105_1402+106insA
XM_017008037.1:c.1009+105_1009+106insA (CYP4V2)	XP_016863526.1:n.1009+105_1009+106insA
NM_207352.4:c.1405+105_1405+106insA (CYP4V2) MANE Select	NP_997235.3:n.1405+105_1405+106insA