Canonical Allele Identifier: CA358950371

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187130261C>G (hg19) ; chr4:g.186209107C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1240C>G (CYP4V2) MANE Select	ENSP00000368079.4:p.Leu414Val
ENST00000378802.4:c.1240C>G (CYP4V2)	ENSP00000368079.4:p.Leu414Val
ENST00000502665.1:n.475C>G (CYP4V2)
ENST00000507209.5:n.5938C>G (CYP4V2)
ENST00000511608.5:c.36C>G (KLKB1)
ENST00000513354.5:n.330C>G (CYP4V2)
NM_207352.3:c.1240C>G (CYP4V2)	NP_997235.3:p.Leu414Val
XM_005262935.2:c.1237C>G (CYP4V2)	XP_005262992.1:p.Leu413Val
XM_006714184.2:c.844C>G (CYP4V2)	XP_006714247.1:p.Leu282Val
XM_005262935.4:c.1237C>G (CYP4V2)	XP_005262992.1:p.Leu413Val
XM_017008037.1:c.844C>G (CYP4V2)	XP_016863526.1:p.Leu282Val
NM_207352.4:c.1240C>G (CYP4V2) MANE Select	NP_997235.3:p.Leu414Val