Canonical Allele Identifier: CA2842537794

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209333G>T , CM000666.2:g.186209333G>T	GRCh38
NC_000004.11:g.187130487G>T , CM000666.1:g.187130487G>T	GRCh37
NC_000004.10:g.187367481G>T	NCBI36
NG_007965.1:g.22814G>T
NG_012095.2:g.5355G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1405+61G>T (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+61G>T
ENST00000378802.4:c.1405+61G>T (CYP4V2)	ENSP00000368079.4:n.1405+61G>T
ENST00000502665.1:n.640+61G>T (CYP4V2)
ENST00000507209.5:n.6103+61G>T (CYP4V2)
ENST00000511608.5:c.201+61G>T (KLKB1)
ENST00000513354.5:n.495+61G>T (CYP4V2)
NM_207352.3:c.1405+61G>T (CYP4V2)	NP_997235.3:n.1405+61G>T
XM_005262935.2:c.1402+61G>T (CYP4V2)	XP_005262992.1:n.1402+61G>T
XM_006714184.2:c.1009+61G>T (CYP4V2)	XP_006714247.1:n.1009+61G>T
XM_005262935.4:c.1402+61G>T (CYP4V2)	XP_005262992.1:n.1402+61G>T
XM_017008037.1:c.1009+61G>T (CYP4V2)	XP_016863526.1:n.1009+61G>T
NM_207352.4:c.1405+61G>T (CYP4V2) MANE Select	NP_997235.3:n.1405+61G>T