Canonical Allele Identifier: CA1519893006

Gene: CYP4V2 KLKB1

Linked Data

• dbSNP Id: rs1736731770

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211772G>A , CM000666.2:g.186211772G>A	GRCh38
NC_000004.11:g.187132926G>A , CM000666.1:g.187132926G>A	GRCh37
NC_000004.10:g.187369920G>A	NCBI36
NG_007965.1:g.25253G>A
NG_012095.2:g.7794G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*1131G>A (CYP4V2) MANE Select	ENSP00000368079.4:n.*1131G>A
ENST00000502665.1:n.1944G>A (CYP4V2)
ENST00000507209.5:n.7407G>A (CYP4V2)
ENST00000511608.5:c.201+2500G>A (KLKB1)
NM_207352.3:c.*1131G>A (CYP4V2)	NP_997235.3:n.*1131G>A
XM_005262935.2:c.*1131G>A (CYP4V2)	XP_005262992.1:n.*1131G>A
XM_006714184.2:c.*1131G>A (CYP4V2)	XP_006714247.1:n.*1131G>A
XM_011531931.1:c.-2937G>A (KLKB1)	XP_011530233.1:n.-2937G>A
XM_011531932.1:c.-3187G>A (KLKB1)	XP_011530234.1:n.-3187G>A
XM_011531933.1:c.-3001G>A (KLKB1)	XP_011530235.1:n.-3001G>A
XM_005262935.4:c.*1131G>A (CYP4V2)	XP_005262992.1:n.*1131G>A
XM_017008037.1:c.*1131G>A (CYP4V2)	XP_016863526.1:n.*1131G>A
NM_207352.4:c.*1131G>A (CYP4V2) MANE Select	NP_997235.3:n.*1131G>A