Canonical Allele Identifier: CA1519892149

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186210677_186210678delinsGT , CM000666.2:g.186210677_186210678delinsGT	GRCh38
NC_000004.11:g.187131831_187131832delinsGT , CM000666.1:g.187131831_187131832delinsGT	GRCh37
NC_000004.10:g.187368825_187368826delinsGT	NCBI36
NG_007965.1:g.24158_24159delinsGT
NG_012095.2:g.6699_6700delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.*36_*37delinsGT (CYP4V2) MANE Select	ENSP00000368079.4:n.*36_*37delinsGT
ENST00000378802.4:c.*36_*37delinsGT (CYP4V2)	ENSP00000368079.4:n.*36_*37delinsGT
ENST00000502665.1:n.849_850delinsGT (CYP4V2)
ENST00000507209.5:n.6312_6313delinsGT (CYP4V2)
ENST00000511608.5:c.201+1405_201+1406delinsGT (KLKB1)
ENST00000513354.5:n.704_705delinsGT (CYP4V2)
NM_207352.3:c.*36_*37delinsGT (CYP4V2)	NP_997235.3:n.*36_*37delinsGT
XM_005262935.2:c.*36_*37delinsGT (CYP4V2)	XP_005262992.1:n.*36_*37delinsGT
XM_006714184.2:c.*36_*37delinsGT (CYP4V2)	XP_006714247.1:n.*36_*37delinsGT
XM_005262935.4:c.*36_*37delinsGT (CYP4V2)	XP_005262992.1:n.*36_*37delinsGT
XM_017008037.1:c.*36_*37delinsGT (CYP4V2)	XP_016863526.1:n.*36_*37delinsGT
NM_207352.4:c.*36_*37delinsGT (CYP4V2) MANE Select	NP_997235.3:n.*36_*37delinsGT