Canonical Allele Identifier: CA358950370

Gene: CYP4V2 KLKB1

Linked Data

• gnomAD v4: 4-186209107-C-A
• MyVariant Identifiers: chr4:g.187130261C>A (hg19) ; chr4:g.186209107C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209107C>A , CM000666.2:g.186209107C>A	GRCh38
NC_000004.11:g.187130261C>A , CM000666.1:g.187130261C>A	GRCh37
NC_000004.10:g.187367255C>A	NCBI36
NG_007965.1:g.22588C>A
NG_012095.2:g.5129C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1240C>A (CYP4V2) MANE Select	ENSP00000368079.4:p.Leu414Ile
ENST00000378802.4:c.1240C>A (CYP4V2)	ENSP00000368079.4:p.Leu414Ile
ENST00000502665.1:n.475C>A (CYP4V2)
ENST00000507209.5:n.5938C>A (CYP4V2)
ENST00000511608.5:c.36C>A (KLKB1)
ENST00000513354.5:n.330C>A (CYP4V2)
NM_207352.3:c.1240C>A (CYP4V2)	NP_997235.3:p.Leu414Ile
XM_005262935.2:c.1237C>A (CYP4V2)	XP_005262992.1:p.Leu413Ile
XM_006714184.2:c.844C>A (CYP4V2)	XP_006714247.1:p.Leu282Ile
XM_005262935.4:c.1237C>A (CYP4V2)	XP_005262992.1:p.Leu413Ile
XM_017008037.1:c.844C>A (CYP4V2)	XP_016863526.1:p.Leu282Ile
NM_207352.4:c.1240C>A (CYP4V2) MANE Select	NP_997235.3:p.Leu414Ile