Canonical Allele Identifier: CA2764868808

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209065_186209066insA , CM000666.2:g.186209065_186209066insA	GRCh38
NC_000004.11:g.187130219_187130220insA , CM000666.1:g.187130219_187130220insA	GRCh37
NC_000004.10:g.187367213_187367214insA	NCBI36
NG_007965.1:g.22546_22547insA
NG_012095.2:g.5087_5088insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1226-28_1226-27insA (CYP4V2) MANE Select	ENSP00000368079.4:n.1226-28_1226-27insA
ENST00000378802.4:c.1226-28_1226-27insA (CYP4V2)	ENSP00000368079.4:n.1226-28_1226-27insA
ENST00000502665.1:n.461-28_461-27insA (CYP4V2)
ENST00000507209.5:n.5924-28_5924-27insA (CYP4V2)
ENST00000511608.5:c.22-28_22-27insA (KLKB1)
ENST00000513354.5:n.316-28_316-27insA (CYP4V2)
NM_207352.3:c.1226-28_1226-27insA (CYP4V2)	NP_997235.3:n.1226-28_1226-27insA
XM_005262935.2:c.1226-31_1226-30insA (CYP4V2)	XP_005262992.1:n.1226-31_1226-30insA
XM_006714184.2:c.830-28_830-27insA (CYP4V2)	XP_006714247.1:n.830-28_830-27insA
XM_005262935.4:c.1226-31_1226-30insA (CYP4V2)	XP_005262992.1:n.1226-31_1226-30insA
XM_017008037.1:c.830-28_830-27insA (CYP4V2)	XP_016863526.1:n.830-28_830-27insA
NM_207352.4:c.1226-28_1226-27insA (CYP4V2) MANE Select	NP_997235.3:n.1226-28_1226-27insA