Canonical Allele Identifier: CA1519891190

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208697_186208753delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT , CM000666.2:g.186208697_186208753delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	GRCh38
NC_000004.11:g.187129851_187129907delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT , CM000666.1:g.187129851_187129907delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	GRCh37
NC_000004.10:g.187366845_187366901delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	NCBI36
NG_007965.1:g.22178_22234delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT
NG_012095.2:g.4719_4775delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1091-168_1091-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT MANE Select	ENSP00000368079.4:n.1091-168_1091-112deli...
ENST00000378802.4:c.1091-168_1091-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	ENSP00000368079.4:n.1091-168_1091-112deli...
ENST00000502665.1:n.326-168_326-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT
ENST00000507209.5:n.5789-168_5789-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT
ENST00000513354.5:n.181-168_181-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT
NM_207352.3:c.1091-168_1091-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	NP_997235.3:n.1091-168_1091-112delinsCATT...
XM_005262935.2:c.1091-168_1091-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	XP_005262992.1:n.1091-168_1091-112delinsC...
XM_006714184.2:c.695-168_695-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	XP_006714247.1:n.695-168_695-112delinsCAT...
XM_005262935.4:c.1091-168_1091-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	XP_005262992.1:n.1091-168_1091-112delinsC...
XM_017008037.1:c.695-168_695-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT	XP_016863526.1:n.695-168_695-112delinsCAT...
NM_207352.4:c.1091-168_1091-112delinsCATTTGATGGGTATTTAGCATCCCCTGCCTTGATCCACGTGTTCTTCTTTGTTGGGT MANE Select	NP_997235.3:n.1091-168_1091-112delinsCATT...