Canonical Allele Identifier: CA2764868909

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209354_186209355insAC , CM000666.2:g.186209354_186209355insAC	GRCh38
NC_000004.11:g.187130508_187130509insAC , CM000666.1:g.187130508_187130509insAC	GRCh37
NC_000004.10:g.187367502_187367503insAC	NCBI36
NG_007965.1:g.22835_22836insAC
NG_012095.2:g.5376_5377insAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1405+82_1405+83insAC (CYP4V2) MANE Select	ENSP00000368079.4:n.1405+82_1405+83insAC
ENST00000378802.4:c.1405+82_1405+83insAC (CYP4V2)	ENSP00000368079.4:n.1405+82_1405+83insAC
ENST00000502665.1:n.640+82_640+83insAC (CYP4V2)
ENST00000507209.5:n.6103+82_6103+83insAC (CYP4V2)
ENST00000511608.5:c.201+82_201+83insAC (KLKB1)
ENST00000513354.5:n.495+82_495+83insAC (CYP4V2)
NM_207352.3:c.1405+82_1405+83insAC (CYP4V2)	NP_997235.3:n.1405+82_1405+83insAC
XM_005262935.2:c.1402+82_1402+83insAC (CYP4V2)	XP_005262992.1:n.1402+82_1402+83insAC
XM_006714184.2:c.1009+82_1009+83insAC (CYP4V2)	XP_006714247.1:n.1009+82_1009+83insAC
XM_005262935.4:c.1402+82_1402+83insAC (CYP4V2)	XP_005262992.1:n.1402+82_1402+83insAC
XM_017008037.1:c.1009+82_1009+83insAC (CYP4V2)	XP_016863526.1:n.1009+82_1009+83insAC
NM_207352.4:c.1405+82_1405+83insAC (CYP4V2) MANE Select	NP_997235.3:n.1405+82_1405+83insAC