Canonical Allele Identifier: CA358950699

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187130418A>C (hg19) ; chr4:g.186209264A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209264A>C , CM000666.2:g.186209264A>C	GRCh38
NC_000004.11:g.187130418A>C , CM000666.1:g.187130418A>C	GRCh37
NC_000004.10:g.187367412A>C	NCBI36
NG_007965.1:g.22745A>C
NG_012095.2:g.5286A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1397A>C (CYP4V2) MANE Select	ENSP00000368079.4:p.Asn466Thr
ENST00000378802.4:c.1397A>C (CYP4V2)	ENSP00000368079.4:p.Asn466Thr
ENST00000502665.1:n.632A>C (CYP4V2)
ENST00000507209.5:n.6095A>C (CYP4V2)
ENST00000511608.5:c.193A>C (KLKB1)
ENST00000513354.5:n.487A>C (CYP4V2)
NM_207352.3:c.1397A>C (CYP4V2)	NP_997235.3:p.Asn466Thr
XM_005262935.2:c.1394A>C (CYP4V2)	XP_005262992.1:p.Asn465Thr
XM_006714184.2:c.1001A>C (CYP4V2)	XP_006714247.1:p.Asn334Thr
XM_005262935.4:c.1394A>C (CYP4V2)	XP_005262992.1:p.Asn465Thr
XM_017008037.1:c.1001A>C (CYP4V2)	XP_016863526.1:p.Asn334Thr
NM_207352.4:c.1397A>C (CYP4V2) MANE Select	NP_997235.3:p.Asn466Thr