Canonical Allele Identifier: CA2764867964

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197694_186197695insACA , CM000666.2:g.186197694_186197695insACA	GRCh38
NC_000004.11:g.187118848_187118849insACA , CM000666.1:g.187118848_187118849insACA	GRCh37
NC_000004.10:g.187355842_187355843insACA	NCBI36
NG_007965.1:g.11175_11176insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+92_674+93insACA MANE Select	ENSP00000368079.4:n.674+92_674+93insACA
ENST00000378802.4:c.674+92_674+93insACA	ENSP00000368079.4:n.674+92_674+93insACA
ENST00000507209.5:n.1515+92_1515+93insACA
NM_207352.3:c.674+92_674+93insACA	NP_997235.3:n.674+92_674+93insACA
XM_005262935.2:c.674+92_674+93insACA	XP_005262992.1:n.674+92_674+93insACA
XM_006714184.2:c.278+92_278+93insACA	XP_006714247.1:n.278+92_278+93insACA
XM_005262935.4:c.674+92_674+93insACA	XP_005262992.1:n.674+92_674+93insACA
XM_017008037.1:c.278+92_278+93insACA	XP_016863526.1:n.278+92_278+93insACA
NM_207352.4:c.674+92_674+93insACA MANE Select	NP_997235.3:n.674+92_674+93insACA