Canonical Allele Identifier: CA2672899373

Gene: CYP4V2 KLKB1

Linked Data

• gnomAD v4: 4-186211554-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211554T>C , CM000666.2:g.186211554T>C	GRCh38
NC_000004.11:g.187132708T>C , CM000666.1:g.187132708T>C	GRCh37
NC_000004.10:g.187369702T>C	NCBI36
NG_007965.1:g.25035T>C
NG_012095.2:g.7576T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*913T>C (CYP4V2) MANE Select	ENSP00000368079.4:n.*913T>C
ENST00000502665.1:n.1726T>C (CYP4V2)
ENST00000507209.5:n.7189T>C (CYP4V2)
ENST00000511608.5:c.201+2282T>C (KLKB1)
NM_207352.3:c.*913T>C (CYP4V2)	NP_997235.3:n.*913T>C
XM_005262935.2:c.*913T>C (CYP4V2)	XP_005262992.1:n.*913T>C
XM_006714184.2:c.*913T>C (CYP4V2)	XP_006714247.1:n.*913T>C
XM_011531931.1:c.-3155T>C (KLKB1)	XP_011530233.1:n.-3155T>C
XM_011531932.1:c.-3405T>C (KLKB1)	XP_011530234.1:n.-3405T>C
XM_011531933.1:c.-3219T>C (KLKB1)	XP_011530235.1:n.-3219T>C
XM_005262935.4:c.*913T>C (CYP4V2)	XP_005262992.1:n.*913T>C
XM_017008037.1:c.*913T>C (CYP4V2)	XP_016863526.1:n.*913T>C
NM_207352.4:c.*913T>C (CYP4V2) MANE Select	NP_997235.3:n.*913T>C