Canonical Allele Identifier: CA1071975417
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186211365A>G , CM000666.2:g.186211365A>G GRCh38
NC_000004.11:g.187132519A>G , CM000666.1:g.187132519A>G GRCh37
NC_000004.10:g.187369513A>G NCBI36
NG_007965.1:g.24846A>G
NG_012095.2:g.7387A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.*724A>G (CYP4V2) MANE Select ENSP00000368079.4:n.*724A>G
ENST00000502665.1:n.1537A>G (CYP4V2)
ENST00000507209.5:n.7000A>G (CYP4V2)
ENST00000511608.5:c.201+2093A>G (KLKB1)
NM_207352.3:c.*724A>G (CYP4V2) NP_997235.3:n.*724A>G
XM_005262935.2:c.*724A>G (CYP4V2) XP_005262992.1:n.*724A>G
XM_006714184.2:c.*724A>G (CYP4V2) XP_006714247.1:n.*724A>G
XM_011531931.1:c.-3344A>G (KLKB1) XP_011530233.1:n.-3344A>G
XM_011531932.1:c.-3594A>G (KLKB1) XP_011530234.1:n.-3594A>G
XM_011531933.1:c.-3408A>G (KLKB1) XP_011530235.1:n.-3408A>G
XM_005262935.4:c.*724A>G (CYP4V2) XP_005262992.1:n.*724A>G
XM_017008037.1:c.*724A>G (CYP4V2) XP_016863526.1:n.*724A>G
NM_207352.4:c.*724A>G (CYP4V2) MANE Select NP_997235.3:n.*724A>G