Canonical Allele Identifier: CA358950395

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187130274A>T (hg19) ; chr4:g.186209120A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209120A>T , CM000666.2:g.186209120A>T	GRCh38
NC_000004.11:g.187130274A>T , CM000666.1:g.187130274A>T	GRCh37
NC_000004.10:g.187367268A>T	NCBI36
NG_007965.1:g.22601A>T
NG_012095.2:g.5142A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1253A>T (CYP4V2) MANE Select	ENSP00000368079.4:p.Glu418Val
ENST00000378802.4:c.1253A>T (CYP4V2)	ENSP00000368079.4:p.Glu418Val
ENST00000502665.1:n.488A>T (CYP4V2)
ENST00000507209.5:n.5951A>T (CYP4V2)
ENST00000511608.5:c.49A>T (KLKB1)
ENST00000513354.5:n.343A>T (CYP4V2)
NM_207352.3:c.1253A>T (CYP4V2)	NP_997235.3:p.Glu418Val
XM_005262935.2:c.1250A>T (CYP4V2)	XP_005262992.1:p.Glu417Val
XM_006714184.2:c.857A>T (CYP4V2)	XP_006714247.1:p.Glu286Val
XM_005262935.4:c.1250A>T (CYP4V2)	XP_005262992.1:p.Glu417Val
XM_017008037.1:c.857A>T (CYP4V2)	XP_016863526.1:p.Glu286Val
NM_207352.4:c.1253A>T (CYP4V2) MANE Select	NP_997235.3:p.Glu418Val