Canonical Allele Identifier: CA358951169

Gene: CYP4V2 KLKB1

Linked Data

• MyVariant Identifiers: chr4:g.187131740G>T (hg19) ; chr4:g.186210586G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210586G>T , CM000666.2:g.186210586G>T	GRCh38
NC_000004.11:g.187131740G>T , CM000666.1:g.187131740G>T	GRCh37
NC_000004.10:g.187368734G>T	NCBI36
NG_007965.1:g.24067G>T
NG_012095.2:g.6608G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1523G>T (CYP4V2) MANE Select	ENSP00000368079.4:p.Arg508Leu
ENST00000378802.4:c.1523G>T (CYP4V2)	ENSP00000368079.4:p.Arg508Leu
ENST00000502665.1:n.758G>T (CYP4V2)
ENST00000507209.5:n.6221G>T (CYP4V2)
ENST00000511608.5:c.201+1314G>T (KLKB1)
ENST00000513354.5:n.613G>T (CYP4V2)
NM_207352.3:c.1523G>T (CYP4V2)	NP_997235.3:p.Arg508Leu
XM_005262935.2:c.1520G>T (CYP4V2)	XP_005262992.1:p.Arg507Leu
XM_006714184.2:c.1127G>T (CYP4V2)	XP_006714247.1:p.Arg376Leu
XM_005262935.4:c.1520G>T (CYP4V2)	XP_005262992.1:p.Arg507Leu
XM_017008037.1:c.1127G>T (CYP4V2)	XP_016863526.1:p.Arg376Leu
NM_207352.4:c.1523G>T (CYP4V2) MANE Select	NP_997235.3:p.Arg508Leu