Canonical Allele Identifier: CA442882368

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187130251T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209097T>G , CM000666.2:g.186209097T>G	GRCh38
NC_000004.11:g.187130251T>G , CM000666.1:g.187130251T>G	GRCh37
NC_000004.10:g.187367245T>G	NCBI36
NG_007965.1:g.22578T>G
NG_012095.2:g.5119T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1230T>G (CYP4V2) MANE Select	ENSP00000368079.4:p.Gly410=
ENST00000378802.4:c.1230T>G (CYP4V2)	ENSP00000368079.4:p.Gly410=
ENST00000502665.1:n.465T>G (CYP4V2)
ENST00000507209.5:n.5928T>G (CYP4V2)
ENST00000511608.5:c.26T>G (KLKB1)
ENST00000513354.5:n.320T>G (CYP4V2)
NM_207352.3:c.1230T>G (CYP4V2)	NP_997235.3:p.Gly410=
XM_005262935.2:c.1227T>G (CYP4V2)	XP_005262992.1:p.Gly409=
XM_006714184.2:c.834T>G (CYP4V2)	XP_006714247.1:p.Gly278=
XM_005262935.4:c.1227T>G (CYP4V2)	XP_005262992.1:p.Gly409=
XM_017008037.1:c.834T>G (CYP4V2)	XP_016863526.1:p.Gly278=
NM_207352.4:c.1230T>G (CYP4V2) MANE Select	NP_997235.3:p.Gly410=