Canonical Allele Identifier: CA2764867669

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204657dup , CM000666.2:g.186204657dup	GRCh38
NC_000004.11:g.187125811dup , CM000666.1:g.187125811dup	GRCh37
NC_000004.10:g.187362805dup	NCBI36
NG_007965.1:g.18138dup
NG_012095.2:g.679dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-543dup MANE Select	ENSP00000368079.4:n.988-543dup
ENST00000378802.4:c.988-543dup	ENSP00000368079.4:n.988-543dup
ENST00000507209.5:n.5143dup
ENST00000513354.5:n.77+200dup
NM_207352.3:c.988-543dup	NP_997235.3:n.988-543dup
XM_005262935.2:c.988-543dup	XP_005262992.1:n.988-543dup
XM_006714184.2:c.592-543dup	XP_006714247.1:n.592-543dup
XM_005262935.4:c.988-543dup	XP_005262992.1:n.988-543dup
XM_017008037.1:c.592-543dup	XP_016863526.1:n.592-543dup
NM_207352.4:c.988-543dup MANE Select	NP_997235.3:n.988-543dup