Canonical Allele Identifier: CA1519919478

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197632_186197635delinsAATT , CM000666.2:g.186197632_186197635delinsAATT	GRCh38
NC_000004.11:g.187118786_187118789delinsAATT , CM000666.1:g.187118786_187118789delinsAATT	GRCh37
NC_000004.10:g.187355780_187355783delinsAATT	NCBI36
NG_007965.1:g.11113_11116delinsAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+30_674+33delinsAATT MANE Select	ENSP00000368079.4:n.674+30_674+33delinsAATT
ENST00000378802.4:c.674+30_674+33delinsAATT	ENSP00000368079.4:n.674+30_674+33delinsAATT
ENST00000507209.5:n.1515+30_1515+33delinsAATT
NM_207352.3:c.674+30_674+33delinsAATT	NP_997235.3:n.674+30_674+33delinsAATT
XM_005262935.2:c.674+30_674+33delinsAATT	XP_005262992.1:n.674+30_674+33delinsAATT
XM_006714184.2:c.278+30_278+33delinsAATT	XP_006714247.1:n.278+30_278+33delinsAATT
XM_005262935.4:c.674+30_674+33delinsAATT	XP_005262992.1:n.674+30_674+33delinsAATT
XM_017008037.1:c.278+30_278+33delinsAATT	XP_016863526.1:n.278+30_278+33delinsAATT
NM_207352.4:c.674+30_674+33delinsAATT MANE Select	NP_997235.3:n.674+30_674+33delinsAATT