Canonical Allele Identifier: CA2764868802
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186209053_186209054insAG , CM000666.2:g.186209053_186209054insAG GRCh38
NC_000004.11:g.187130207_187130208insAG , CM000666.1:g.187130207_187130208insAG GRCh37
NC_000004.10:g.187367201_187367202insAG NCBI36
NG_007965.1:g.22534_22535insAG
NG_012095.2:g.5075_5076insAG

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1226-40_1226-39insAG (CYP4V2) MANE Select ENSP00000368079.4:n.1226-40_1226-39insAG
ENST00000378802.4:c.1226-40_1226-39insAG (CYP4V2) ENSP00000368079.4:n.1226-40_1226-39insAG
ENST00000502665.1:n.461-40_461-39insAG (CYP4V2)
ENST00000507209.5:n.5924-40_5924-39insAG (CYP4V2)
ENST00000511608.5:c.22-40_22-39insAG (KLKB1)
ENST00000513354.5:n.316-40_316-39insAG (CYP4V2)
NM_207352.3:c.1226-40_1226-39insAG (CYP4V2) NP_997235.3:n.1226-40_1226-39insAG
XM_005262935.2:c.1226-43_1226-42insAG (CYP4V2) XP_005262992.1:n.1226-43_1226-42insAG
XM_006714184.2:c.830-40_830-39insAG (CYP4V2) XP_006714247.1:n.830-40_830-39insAG
XM_005262935.4:c.1226-43_1226-42insAG (CYP4V2) XP_005262992.1:n.1226-43_1226-42insAG
XM_017008037.1:c.830-40_830-39insAG (CYP4V2) XP_016863526.1:n.830-40_830-39insAG
NM_207352.4:c.1226-40_1226-39insAG (CYP4V2) MANE Select NP_997235.3:n.1226-40_1226-39insAG
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