Canonical Allele Identifier: CA2764867830

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204747_186204748insA , CM000666.2:g.186204747_186204748insA	GRCh38
NC_000004.11:g.187125901_187125902insA , CM000666.1:g.187125901_187125902insA	GRCh37
NC_000004.10:g.187362895_187362896insA	NCBI36
NG_007965.1:g.18228_18229insA
NG_012095.2:g.769_770insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-453_988-452insA MANE Select	ENSP00000368079.4:n.988-453_988-452insA
ENST00000378802.4:c.988-453_988-452insA	ENSP00000368079.4:n.988-453_988-452insA
ENST00000507209.5:n.5233_5234insA
ENST00000513354.5:n.77+290_77+291insA
NM_207352.3:c.988-453_988-452insA	NP_997235.3:n.988-453_988-452insA
XM_005262935.2:c.988-453_988-452insA	XP_005262992.1:n.988-453_988-452insA
XM_006714184.2:c.592-453_592-452insA	XP_006714247.1:n.592-453_592-452insA
XM_005262935.4:c.988-453_988-452insA	XP_005262992.1:n.988-453_988-452insA
XM_017008037.1:c.592-453_592-452insA	XP_016863526.1:n.592-453_592-452insA
NM_207352.4:c.988-453_988-452insA MANE Select	NP_997235.3:n.988-453_988-452insA