Canonical Allele Identifier: CA2764867936

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197659_186197660insAGA , CM000666.2:g.186197659_186197660insAGA	GRCh38
NC_000004.11:g.187118813_187118814insAGA , CM000666.1:g.187118813_187118814insAGA	GRCh37
NC_000004.10:g.187355807_187355808insAGA	NCBI36
NG_007965.1:g.11140_11141insAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+57_674+58insAGA MANE Select	ENSP00000368079.4:n.674+57_674+58insAGA
ENST00000378802.4:c.674+57_674+58insAGA	ENSP00000368079.4:n.674+57_674+58insAGA
ENST00000507209.5:n.1515+57_1515+58insAGA
NM_207352.3:c.674+57_674+58insAGA	NP_997235.3:n.674+57_674+58insAGA
XM_005262935.2:c.674+57_674+58insAGA	XP_005262992.1:n.674+57_674+58insAGA
XM_006714184.2:c.278+57_278+58insAGA	XP_006714247.1:n.278+57_278+58insAGA
XM_005262935.4:c.674+57_674+58insAGA	XP_005262992.1:n.674+57_674+58insAGA
XM_017008037.1:c.278+57_278+58insAGA	XP_016863526.1:n.278+57_278+58insAGA
NM_207352.4:c.674+57_674+58insAGA MANE Select	NP_997235.3:n.674+57_674+58insAGA