Canonical Allele Identifier: CA1519915295

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194638_186194639delinsAT , CM000666.2:g.186194638_186194639delinsAT	GRCh38
NC_000004.11:g.187115792_187115793delinsAT , CM000666.1:g.187115792_187115793delinsAT	GRCh37
NC_000004.10:g.187352786_187352787delinsAT	NCBI36
NG_007965.1:g.8119_8120delinsAT

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.327+26_327+27delinsAT MANE Select	ENSP00000368079.4:n.327+26_327+27delinsAT...
ENST00000378802.4:c.327+26_327+27delinsAT	ENSP00000368079.4:n.327+26_327+27delinsAT...
NM_207352.3:c.327+26_327+27delinsAT	NP_997235.3:n.327+26_327+27delinsAT
XM_005262935.2:c.327+26_327+27delinsAT	XP_005262992.1:n.327+26_327+27delinsAT
XM_006714184.2:c.17+26_17+27delinsAT	XP_006714247.1:n.17+26_17+27delinsAT
XM_005262935.4:c.327+26_327+27delinsAT	XP_005262992.1:n.327+26_327+27delinsAT
XM_017008037.1:c.17+26_17+27delinsAT	XP_016863526.1:n.17+26_17+27delinsAT
NM_207352.4:c.327+26_327+27delinsAT MANE Select	NP_997235.3:n.327+26_327+27delinsAT