Canonical Allele Identifier: CA276932

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209263A>G , CM000666.2:g.186209263A>G	GRCh38
NC_000004.11:g.187130417A>G , CM000666.1:g.187130417A>G	GRCh37
NC_000004.10:g.187367411A>G	NCBI36
NG_007965.1:g.22744A>G
NG_012095.2:g.5285A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_207352.4:c.1396A>G (CYP4V2) MANE Select	NP_997235.3:p.Asn466Asp
ENST00000378802.5:c.1396A>G (CYP4V2) MANE Select	ENSP00000368079.4:p.Asn466Asp
NM_207352.3:c.1396A>G (CYP4V2)	NP_997235.3:p.Asn466Asp
ENST00000378802.4:c.1396A>G (CYP4V2)	ENSP00000368079.4:p.Asn466Asp
ENST00000502665.1:n.631A>G (CYP4V2)
ENST00000507209.5:n.6094A>G (CYP4V2)
ENST00000511608.5:c.192A>G (KLKB1)
ENST00000513354.5:n.486A>G (CYP4V2)
XM_005262935.2:c.1393A>G (CYP4V2)	XP_005262992.1:p.Asn465Asp
XM_005262935.4:c.1393A>G (CYP4V2)	XP_005262992.1:p.Asn465Asp
XM_006714184.2:c.1000A>G (CYP4V2)	XP_006714247.1:p.Asn334Asp
XM_017008037.1:c.1000A>G (CYP4V2)	XP_016863526.1:p.Asn334Asp