Canonical Allele Identifier: CA2764867929

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186197634_186197635insA , CM000666.2:g.186197634_186197635insA	GRCh38
NC_000004.11:g.187118788_187118789insA , CM000666.1:g.187118788_187118789insA	GRCh37
NC_000004.10:g.187355782_187355783insA	NCBI36
NG_007965.1:g.11115_11116insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.674+32_674+33insA MANE Select	ENSP00000368079.4:n.674+32_674+33insA
ENST00000378802.4:c.674+32_674+33insA	ENSP00000368079.4:n.674+32_674+33insA
ENST00000507209.5:n.1515+32_1515+33insA
NM_207352.3:c.674+32_674+33insA	NP_997235.3:n.674+32_674+33insA
XM_005262935.2:c.674+32_674+33insA	XP_005262992.1:n.674+32_674+33insA
XM_006714184.2:c.278+32_278+33insA	XP_006714247.1:n.278+32_278+33insA
XM_005262935.4:c.674+32_674+33insA	XP_005262992.1:n.674+32_674+33insA
XM_017008037.1:c.278+32_278+33insA	XP_016863526.1:n.278+32_278+33insA
NM_207352.4:c.674+32_674+33insA MANE Select	NP_997235.3:n.674+32_674+33insA