Canonical Allele Identifier: CA2672899306

Gene: CYP4V2 KLKB1

Linked Data

• gnomAD v4: 4-186211520-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186211520G>T , CM000666.2:g.186211520G>T	GRCh38
NC_000004.11:g.187132674G>T , CM000666.1:g.187132674G>T	GRCh37
NC_000004.10:g.187369668G>T	NCBI36
NG_007965.1:g.25001G>T
NG_012095.2:g.7542G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.*879G>T (CYP4V2) MANE Select	ENSP00000368079.4:n.*879G>T
ENST00000502665.1:n.1692G>T (CYP4V2)
ENST00000507209.5:n.7155G>T (CYP4V2)
ENST00000511608.5:c.201+2248G>T (KLKB1)
NM_207352.3:c.*879G>T (CYP4V2)	NP_997235.3:n.*879G>T
XM_005262935.2:c.*879G>T (CYP4V2)	XP_005262992.1:n.*879G>T
XM_006714184.2:c.*879G>T (CYP4V2)	XP_006714247.1:n.*879G>T
XM_011531931.1:c.-3189G>T (KLKB1)	XP_011530233.1:n.-3189G>T
XM_011531932.1:c.-3439G>T (KLKB1)	XP_011530234.1:n.-3439G>T
XM_011531933.1:c.-3253G>T (KLKB1)	XP_011530235.1:n.-3253G>T
XM_005262935.4:c.*879G>T (CYP4V2)	XP_005262992.1:n.*879G>T
XM_017008037.1:c.*879G>T (CYP4V2)	XP_016863526.1:n.*879G>T
NM_207352.4:c.*879G>T (CYP4V2) MANE Select	NP_997235.3:n.*879G>T