Canonical Allele Identifier: CA1519914548

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186194206_186194210delinsTAGAA , CM000666.2:g.186194206_186194210delinsTAGAA	GRCh38
NC_000004.11:g.187115360_187115364delinsTAGAA , CM000666.1:g.187115360_187115364delinsTAGAA	GRCh37
NC_000004.10:g.187352354_187352358delinsTAGAA	NCBI36
NG_007965.1:g.7687_7691delinsTAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.215-294_215-290delinsTAGAA MANE Select	ENSP00000368079.4:n.215-294_215-290delinsTAGAA
ENST00000378802.4:c.215-294_215-290delinsTAGAA	ENSP00000368079.4:n.215-294_215-290delinsTAGAA
NM_207352.3:c.215-294_215-290delinsTAGAA	NP_997235.3:n.215-294_215-290delinsTAGAA
XM_005262935.2:c.215-294_215-290delinsTAGAA	XP_005262992.1:n.215-294_215-290delinsTAGAA
XM_005262935.4:c.215-294_215-290delinsTAGAA	XP_005262992.1:n.215-294_215-290delinsTAGAA
XM_017008037.1:c.-96-294_-96-290delinsTAGAA	XP_016863526.1:n.-96-294_-96-290delinsTAGAA
NM_207352.4:c.215-294_215-290delinsTAGAA MANE Select	NP_997235.3:n.215-294_215-290delinsTAGAA