Canonical Allele Identifier: CA2764867958

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197690_186197691insAG , CM000666.2:g.186197690_186197691insAG	GRCh38
NC_000004.11:g.187118844_187118845insAG , CM000666.1:g.187118844_187118845insAG	GRCh37
NC_000004.10:g.187355838_187355839insAG	NCBI36
NG_007965.1:g.11171_11172insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+88_674+89insAG MANE Select	ENSP00000368079.4:n.674+88_674+89insAG
ENST00000378802.4:c.674+88_674+89insAG	ENSP00000368079.4:n.674+88_674+89insAG
ENST00000507209.5:n.1515+88_1515+89insAG
NM_207352.3:c.674+88_674+89insAG	NP_997235.3:n.674+88_674+89insAG
XM_005262935.2:c.674+88_674+89insAG	XP_005262992.1:n.674+88_674+89insAG
XM_006714184.2:c.278+88_278+89insAG	XP_006714247.1:n.278+88_278+89insAG
XM_005262935.4:c.674+88_674+89insAG	XP_005262992.1:n.674+88_674+89insAG
XM_017008037.1:c.278+88_278+89insAG	XP_016863526.1:n.278+88_278+89insAG
NM_207352.4:c.674+88_674+89insAG MANE Select	NP_997235.3:n.674+88_674+89insAG