Canonical Allele Identifier: CA2672897591
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209079_186209091del , CM000666.2:g.186209079_186209091del GRCh38
NC_000004.11:g.187130233_187130245del , CM000666.1:g.187130233_187130245del GRCh37
NC_000004.10:g.187367227_187367239del NCBI36
NG_007965.1:g.22560_22572del
NG_012095.2:g.5101_5113del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1226-14_1226-2del (CYP4V2) MANE Select ENSP00000368079.4:n.1226-14_1226-2del
ENST00000378802.4:c.1226-14_1226-2del (CYP4V2) ENSP00000368079.4:n.1226-14_1226-2del
ENST00000502665.1:n.461-14_461-2del (CYP4V2)
ENST00000507209.5:n.5924-14_5924-2del (CYP4V2)
ENST00000511608.5:c.22-14_22-2del (KLKB1)
ENST00000513354.5:n.316-14_316-2del (CYP4V2)
NM_207352.3:c.1226-14_1226-2del (CYP4V2) NP_997235.3:n.1226-14_1226-2del
XM_005262935.2:c.1226-17_1226-5del (CYP4V2) XP_005262992.1:n.1226-17_1226-5del
XM_006714184.2:c.830-14_830-2del (CYP4V2) XP_006714247.1:n.830-14_830-2del
XM_005262935.4:c.1226-17_1226-5del (CYP4V2) XP_005262992.1:n.1226-17_1226-5del
XM_017008037.1:c.830-14_830-2del (CYP4V2) XP_016863526.1:n.830-14_830-2del
NM_207352.4:c.1226-14_1226-2del (CYP4V2) MANE Select NP_997235.3:n.1226-14_1226-2del