Canonical Allele Identifier: CA2764867941

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186205301_186205302insACA , CM000666.2:g.186205301_186205302insACA	GRCh38
NC_000004.11:g.187126455_187126456insACA , CM000666.1:g.187126455_187126456insACA	GRCh37
NC_000004.10:g.187363449_187363450insACA	NCBI36
NG_007965.1:g.18782_18783insACA
NG_012095.2:g.1323_1324insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1089_1090insACA MANE Select	ENSP00000368079.4:p.Phe363_Gly364insThr
ENST00000378802.4:c.1089_1090insACA	ENSP00000368079.4:p.Phe363_Gly364insThr
ENST00000502665.1:n.324_325insACA
ENST00000507209.5:n.5787_5788insACA
ENST00000513354.5:n.179_180insACA
NM_207352.3:c.1089_1090insACA	NP_997235.3:p.Phe363_Gly364insThr
XM_005262935.2:c.1089_1090insACA	XP_005262992.1:p.Phe363_Gly364insThr
XM_006714184.2:c.693_694insACA	XP_006714247.1:p.Phe231_Gly232insThr
XM_005262935.4:c.1089_1090insACA	XP_005262992.1:p.Phe363_Gly364insThr
XM_017008037.1:c.693_694insACA	XP_016863526.1:p.Phe231_Gly232insThr
NM_207352.4:c.1089_1090insACA MANE Select	NP_997235.3:p.Phe363_Gly364insThr