Canonical Allele Identifier: CA2764868877

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209303_186209304del , CM000666.2:g.186209303_186209304del	GRCh38
NC_000004.11:g.187130457_187130458del , CM000666.1:g.187130457_187130458del	GRCh37
NC_000004.10:g.187367451_187367452del	NCBI36
NG_007965.1:g.22784_22785del
NG_012095.2:g.5325_5326del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1405+31_1405+32del (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+31_1405+32del
ENST00000378802.4:c.1405+31_1405+32del (CYP4V2)	ENSP00000368079.4:n.1405+31_1405+32del
ENST00000502665.1:n.640+31_640+32del (CYP4V2)
ENST00000507209.5:n.6103+31_6103+32del (CYP4V2)
ENST00000511608.5:c.201+31_201+32del (KLKB1)
ENST00000513354.5:n.495+31_495+32del (CYP4V2)
NM_207352.3:c.1405+31_1405+32del (CYP4V2)	NP_997235.3:n.1405+31_1405+32del
XM_005262935.2:c.1402+31_1402+32del (CYP4V2)	XP_005262992.1:n.1402+31_1402+32del
XM_006714184.2:c.1009+31_1009+32del (CYP4V2)	XP_006714247.1:n.1009+31_1009+32del
XM_005262935.4:c.1402+31_1402+32del (CYP4V2)	XP_005262992.1:n.1402+31_1402+32del
XM_017008037.1:c.1009+31_1009+32del (CYP4V2)	XP_016863526.1:n.1009+31_1009+32del
NM_207352.4:c.1405+31_1405+32del (CYP4V2) MANE Select	NP_997235.3:n.1405+31_1405+32del