Canonical Allele Identifier: CA2672899013

Gene: CYP4V2 KLKB1

Linked Data

• gnomAD v4: 4-186211390-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211390T>G , CM000666.2:g.186211390T>G	GRCh38
NC_000004.11:g.187132544T>G , CM000666.1:g.187132544T>G	GRCh37
NC_000004.10:g.187369538T>G	NCBI36
NG_007965.1:g.24871T>G
NG_012095.2:g.7412T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*749T>G (CYP4V2) MANE Select	ENSP00000368079.4:n.*749T>G
ENST00000502665.1:n.1562T>G (CYP4V2)
ENST00000507209.5:n.7025T>G (CYP4V2)
ENST00000511608.5:c.201+2118T>G (KLKB1)
NM_207352.3:c.*749T>G (CYP4V2)	NP_997235.3:n.*749T>G
XM_005262935.2:c.*749T>G (CYP4V2)	XP_005262992.1:n.*749T>G
XM_006714184.2:c.*749T>G (CYP4V2)	XP_006714247.1:n.*749T>G
XM_011531931.1:c.-3319T>G (KLKB1)	XP_011530233.1:n.-3319T>G
XM_011531932.1:c.-3569T>G (KLKB1)	XP_011530234.1:n.-3569T>G
XM_011531933.1:c.-3383T>G (KLKB1)	XP_011530235.1:n.-3383T>G
XM_005262935.4:c.*749T>G (CYP4V2)	XP_005262992.1:n.*749T>G
XM_017008037.1:c.*749T>G (CYP4V2)	XP_016863526.1:n.*749T>G
NM_207352.4:c.*749T>G (CYP4V2) MANE Select	NP_997235.3:n.*749T>G