Canonical Allele Identifier: CA358951385

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187131776G>C (hg19) ; chr4:g.186210622G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210622G>C , CM000666.2:g.186210622G>C	GRCh38
NC_000004.11:g.187131776G>C , CM000666.1:g.187131776G>C	GRCh37
NC_000004.10:g.187368770G>C	NCBI36
NG_007965.1:g.24103G>C
NG_012095.2:g.6644G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1559G>C (CYP4V2) MANE Select	ENSP00000368079.4:p.Arg520Thr
ENST00000378802.4:c.1559G>C (CYP4V2)	ENSP00000368079.4:p.Arg520Thr
ENST00000502665.1:n.794G>C (CYP4V2)
ENST00000507209.5:n.6257G>C (CYP4V2)
ENST00000511608.5:c.201+1350G>C (KLKB1)
ENST00000513354.5:n.649G>C (CYP4V2)
NM_207352.3:c.1559G>C (CYP4V2)	NP_997235.3:p.Arg520Thr
XM_005262935.2:c.1556G>C (CYP4V2)	XP_005262992.1:p.Arg519Thr
XM_006714184.2:c.1163G>C (CYP4V2)	XP_006714247.1:p.Arg388Thr
XM_005262935.4:c.1556G>C (CYP4V2)	XP_005262992.1:p.Arg519Thr
XM_017008037.1:c.1163G>C (CYP4V2)	XP_016863526.1:p.Arg388Thr
NM_207352.4:c.1559G>C (CYP4V2) MANE Select	NP_997235.3:p.Arg520Thr