Canonical Allele Identifier: CA2764868937

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209407_186209411del , CM000666.2:g.186209407_186209411del	GRCh38
NC_000004.11:g.187130561_187130565del , CM000666.1:g.187130561_187130565del	GRCh37
NC_000004.10:g.187367555_187367559del	NCBI36
NG_007965.1:g.22888_22892del
NG_012095.2:g.5429_5433del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1405+135_1405+139del (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+135_1405+139del
ENST00000378802.4:c.1405+135_1405+139del (CYP4V2)	ENSP00000368079.4:n.1405+135_1405+139del
ENST00000502665.1:n.640+135_640+139del (CYP4V2)
ENST00000507209.5:n.6103+135_6103+139del (CYP4V2)
ENST00000511608.5:c.201+135_201+139del (KLKB1)
ENST00000513354.5:n.495+135_495+139del (CYP4V2)
NM_207352.3:c.1405+135_1405+139del (CYP4V2)	NP_997235.3:n.1405+135_1405+139del
XM_005262935.2:c.1402+135_1402+139del (CYP4V2)	XP_005262992.1:n.1402+135_1402+139del
XM_006714184.2:c.1009+135_1009+139del (CYP4V2)	XP_006714247.1:n.1009+135_1009+139del
XM_005262935.4:c.1402+135_1402+139del (CYP4V2)	XP_005262992.1:n.1402+135_1402+139del
XM_017008037.1:c.1009+135_1009+139del (CYP4V2)	XP_016863526.1:n.1009+135_1009+139del
NM_207352.4:c.1405+135_1405+139del (CYP4V2) MANE Select	NP_997235.3:n.1405+135_1405+139del