Canonical Allele Identifier: CA2764868782

Gene: CYP4V2 KLKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186209030_186209031insT , CM000666.2:g.186209030_186209031insT	GRCh38
NC_000004.11:g.187130184_187130185insT , CM000666.1:g.187130184_187130185insT	GRCh37
NC_000004.10:g.187367178_187367179insT	NCBI36
NG_007965.1:g.22511_22512insT
NG_012095.2:g.5052_5053insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1225+31_1225+32insT (CYP4V2) MANE Select	ENSP00000368079.4:n.1225+31_1225+32insT
ENST00000378802.4:c.1225+31_1225+32insT (CYP4V2)	ENSP00000368079.4:n.1225+31_1225+32insT
ENST00000502665.1:n.460+31_460+32insT (CYP4V2)
ENST00000507209.5:n.5923+31_5923+32insT (CYP4V2)
ENST00000511608.5:c.21+31_21+32insT (KLKB1)
ENST00000513354.5:n.315+31_315+32insT (CYP4V2)
NM_207352.3:c.1225+31_1225+32insT (CYP4V2)	NP_997235.3:n.1225+31_1225+32insT
XM_005262935.2:c.1225+31_1225+32insT (CYP4V2)	XP_005262992.1:n.1225+31_1225+32insT
XM_006714184.2:c.829+31_829+32insT (CYP4V2)	XP_006714247.1:n.829+31_829+32insT
XM_005262935.4:c.1225+31_1225+32insT (CYP4V2)	XP_005262992.1:n.1225+31_1225+32insT
XM_017008037.1:c.829+31_829+32insT (CYP4V2)	XP_016863526.1:n.829+31_829+32insT
NM_207352.4:c.1225+31_1225+32insT (CYP4V2) MANE Select	NP_997235.3:n.1225+31_1225+32insT