Canonical Allele Identifier: CA2672897914

Gene: CYP4V2 KLKB1

Linked Data

• gnomAD v4: 4-186209311-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209311A>T , CM000666.2:g.186209311A>T	GRCh38
NC_000004.11:g.187130465A>T , CM000666.1:g.187130465A>T	GRCh37
NC_000004.10:g.187367459A>T	NCBI36
NG_007965.1:g.22792A>T
NG_012095.2:g.5333A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1405+39A>T (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+39A>T
ENST00000378802.4:c.1405+39A>T (CYP4V2)	ENSP00000368079.4:n.1405+39A>T
ENST00000502665.1:n.640+39A>T (CYP4V2)
ENST00000507209.5:n.6103+39A>T (CYP4V2)
ENST00000511608.5:c.201+39A>T (KLKB1)
ENST00000513354.5:n.495+39A>T (CYP4V2)
NM_207352.3:c.1405+39A>T (CYP4V2)	NP_997235.3:n.1405+39A>T
XM_005262935.2:c.1402+39A>T (CYP4V2)	XP_005262992.1:n.1402+39A>T
XM_006714184.2:c.1009+39A>T (CYP4V2)	XP_006714247.1:n.1009+39A>T
XM_005262935.4:c.1402+39A>T (CYP4V2)	XP_005262992.1:n.1402+39A>T
XM_017008037.1:c.1009+39A>T (CYP4V2)	XP_016863526.1:n.1009+39A>T
NM_207352.4:c.1405+39A>T (CYP4V2) MANE Select	NP_997235.3:n.1405+39A>T