Canonical Allele Identifier: CA358951450

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187131786T>G (hg19) ; chr4:g.186210632T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210632T>G , CM000666.2:g.186210632T>G	GRCh38
NC_000004.11:g.187131786T>G , CM000666.1:g.187131786T>G	GRCh37
NC_000004.10:g.187368780T>G	NCBI36
NG_007965.1:g.24113T>G
NG_012095.2:g.6654T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1569T>G (CYP4V2) MANE Select	ENSP00000368079.4:p.Asp523Glu
ENST00000378802.4:c.1569T>G (CYP4V2)	ENSP00000368079.4:p.Asp523Glu
ENST00000502665.1:n.804T>G (CYP4V2)
ENST00000507209.5:n.6267T>G (CYP4V2)
ENST00000511608.5:c.201+1360T>G (KLKB1)
ENST00000513354.5:n.659T>G (CYP4V2)
NM_207352.3:c.1569T>G (CYP4V2)	NP_997235.3:p.Asp523Glu
XM_005262935.2:c.1566T>G (CYP4V2)	XP_005262992.1:p.Asp522Glu
XM_006714184.2:c.1173T>G (CYP4V2)	XP_006714247.1:p.Asp391Glu
XM_005262935.4:c.1566T>G (CYP4V2)	XP_005262992.1:p.Asp522Glu
XM_017008037.1:c.1173T>G (CYP4V2)	XP_016863526.1:p.Asp391Glu
NM_207352.4:c.1569T>G (CYP4V2) MANE Select	NP_997235.3:p.Asp523Glu