Canonical Allele Identifier: CA2672899540

Gene: CYP4V2 KLKB1

Linked Data

• gnomAD v4: 4-186211663-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211663A>G , CM000666.2:g.186211663A>G	GRCh38
NC_000004.11:g.187132817A>G , CM000666.1:g.187132817A>G	GRCh37
NC_000004.10:g.187369811A>G	NCBI36
NG_007965.1:g.25144A>G
NG_012095.2:g.7685A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*1022A>G (CYP4V2) MANE Select	ENSP00000368079.4:n.*1022A>G
ENST00000502665.1:n.1835A>G (CYP4V2)
ENST00000507209.5:n.7298A>G (CYP4V2)
ENST00000511608.5:c.201+2391A>G (KLKB1)
NM_207352.3:c.*1022A>G (CYP4V2)	NP_997235.3:n.*1022A>G
XM_005262935.2:c.*1022A>G (CYP4V2)	XP_005262992.1:n.*1022A>G
XM_006714184.2:c.*1022A>G (CYP4V2)	XP_006714247.1:n.*1022A>G
XM_011531931.1:c.-3046A>G (KLKB1)	XP_011530233.1:n.-3046A>G
XM_011531932.1:c.-3296A>G (KLKB1)	XP_011530234.1:n.-3296A>G
XM_011531933.1:c.-3110A>G (KLKB1)	XP_011530235.1:n.-3110A>G
XM_005262935.4:c.*1022A>G (CYP4V2)	XP_005262992.1:n.*1022A>G
XM_017008037.1:c.*1022A>G (CYP4V2)	XP_016863526.1:n.*1022A>G
NM_207352.4:c.*1022A>G (CYP4V2) MANE Select	NP_997235.3:n.*1022A>G