Canonical Allele Identifier: CA358950835

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187131670C>A (hg19) ; chr4:g.186210516C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210516C>A , CM000666.2:g.186210516C>A	GRCh38
NC_000004.11:g.187131670C>A , CM000666.1:g.187131670C>A	GRCh37
NC_000004.10:g.187368664C>A	NCBI36
NG_007965.1:g.23997C>A
NG_012095.2:g.6538C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1453C>A (CYP4V2) MANE Select	ENSP00000368079.4:p.Leu485Met
ENST00000378802.4:c.1453C>A (CYP4V2)	ENSP00000368079.4:p.Leu485Met
ENST00000502665.1:n.688C>A (CYP4V2)
ENST00000507209.5:n.6151C>A (CYP4V2)
ENST00000511608.5:c.201+1244C>A (KLKB1)
ENST00000513354.5:n.543C>A (CYP4V2)
NM_207352.3:c.1453C>A (CYP4V2)	NP_997235.3:p.Leu485Met
XM_005262935.2:c.1450C>A (CYP4V2)	XP_005262992.1:p.Leu484Met
XM_006714184.2:c.1057C>A (CYP4V2)	XP_006714247.1:p.Leu353Met
XM_005262935.4:c.1450C>A (CYP4V2)	XP_005262992.1:p.Leu484Met
XM_017008037.1:c.1057C>A (CYP4V2)	XP_016863526.1:p.Leu353Met
NM_207352.4:c.1453C>A (CYP4V2) MANE Select	NP_997235.3:p.Leu485Met