Canonical Allele Identifier: CA1519893629
Gene: CYP4V2 HGNC NCBI
KLKB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186212568T= , CM000666.2:g.186212568T= GRCh38
NC_000004.11:g.187133722T= , CM000666.1:g.187133722T= GRCh37
NC_000004.10:g.187370716T= NCBI36
NG_007965.1:g.26049T=
NG_012095.2:g.8590T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.*1927T= (CYP4V2) MANE Select ENSP00000368079.4:n.*1927T=
ENST00000502665.1:n.2740T= (CYP4V2)
ENST00000507209.5:n.8203T= (CYP4V2)
ENST00000511608.5:c.201+3296T= (KLKB1)
NM_207352.3:c.*1927T= (CYP4V2) NP_997235.3:n.*1927T=
XM_005262935.2:c.*1927T= (CYP4V2) XP_005262992.1:n.*1927T=
XM_006714184.2:c.*1927T= (CYP4V2) XP_006714247.1:n.*1927T=
XM_011531931.1:c.-2141T= (KLKB1) XP_011530233.1:n.-2141T=
XM_011531932.1:c.-2391T= (KLKB1) XP_011530234.1:n.-2391T=
XM_011531933.1:c.-2205T= (KLKB1) XP_011530235.1:n.-2205T=
XM_005262935.4:c.*1927T= (CYP4V2) XP_005262992.1:n.*1927T=
XM_017008037.1:c.*1927T= (CYP4V2) XP_016863526.1:n.*1927T=
NM_207352.4:c.*1927T= (CYP4V2) MANE Select NP_997235.3:n.*1927T=