Canonical Allele Identifier: CA358950307

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187130142A>T (hg19) ; chr4:g.186208988A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208988A>T , CM000666.2:g.186208988A>T	GRCh38
NC_000004.11:g.187130142A>T , CM000666.1:g.187130142A>T	GRCh37
NC_000004.10:g.187367136A>T	NCBI36
NG_007965.1:g.22469A>T
NG_012095.2:g.5010A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1214A>T (CYP4V2) MANE Select	ENSP00000368079.4:p.Asp405Val
ENST00000378802.4:c.1214A>T (CYP4V2)	ENSP00000368079.4:p.Asp405Val
ENST00000502665.1:n.449A>T (CYP4V2)
ENST00000507209.5:n.5912A>T (CYP4V2)
ENST00000511608.5:c.10A>T (KLKB1)
ENST00000513354.5:n.304A>T (CYP4V2)
NM_207352.3:c.1214A>T (CYP4V2)	NP_997235.3:p.Asp405Val
XM_005262935.2:c.1214A>T (CYP4V2)	XP_005262992.1:p.Asp405Val
XM_006714184.2:c.818A>T (CYP4V2)	XP_006714247.1:p.Asp273Val
XM_005262935.4:c.1214A>T (CYP4V2)	XP_005262992.1:p.Asp405Val
XM_017008037.1:c.818A>T (CYP4V2)	XP_016863526.1:p.Asp273Val
NM_207352.4:c.1214A>T (CYP4V2) MANE Select	NP_997235.3:p.Asp405Val