Canonical Allele Identifier: CA2764867792

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204726_186204727insA , CM000666.2:g.186204726_186204727insA	GRCh38
NC_000004.11:g.187125880_187125881insA , CM000666.1:g.187125880_187125881insA	GRCh37
NC_000004.10:g.187362874_187362875insA	NCBI36
NG_007965.1:g.18207_18208insA
NG_012095.2:g.748_749insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-474_988-473insA MANE Select	ENSP00000368079.4:n.988-474_988-473insA
ENST00000378802.4:c.988-474_988-473insA	ENSP00000368079.4:n.988-474_988-473insA
ENST00000507209.5:n.5212_5213insA
ENST00000513354.5:n.77+269_77+270insA
NM_207352.3:c.988-474_988-473insA	NP_997235.3:n.988-474_988-473insA
XM_005262935.2:c.988-474_988-473insA	XP_005262992.1:n.988-474_988-473insA
XM_006714184.2:c.592-474_592-473insA	XP_006714247.1:n.592-474_592-473insA
XM_005262935.4:c.988-474_988-473insA	XP_005262992.1:n.988-474_988-473insA
XM_017008037.1:c.592-474_592-473insA	XP_016863526.1:n.592-474_592-473insA
NM_207352.4:c.988-474_988-473insA MANE Select	NP_997235.3:n.988-474_988-473insA