Canonical Allele Identifier: CA1519888439

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1736444087

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204705_186204708dup , CM000666.2:g.186204705_186204708dup	GRCh38
NC_000004.11:g.187125859_187125862dup , CM000666.1:g.187125859_187125862dup	GRCh37
NC_000004.10:g.187362853_187362856dup	NCBI36
NG_007965.1:g.18186_18189dup
NG_012095.2:g.727_730dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-495_988-492dup MANE Select	ENSP00000368079.4:n.988-495_988-492dup
ENST00000378802.4:c.988-495_988-492dup	ENSP00000368079.4:n.988-495_988-492dup
ENST00000507209.5:n.5191_5194dup
ENST00000513354.5:n.77+248_77+251dup
NM_207352.3:c.988-495_988-492dup	NP_997235.3:n.988-495_988-492dup
XM_005262935.2:c.988-495_988-492dup	XP_005262992.1:n.988-495_988-492dup
XM_006714184.2:c.592-495_592-492dup	XP_006714247.1:n.592-495_592-492dup
XM_005262935.4:c.988-495_988-492dup	XP_005262992.1:n.988-495_988-492dup
XM_017008037.1:c.592-495_592-492dup	XP_016863526.1:n.592-495_592-492dup
NM_207352.4:c.988-495_988-492dup MANE Select	NP_997235.3:n.988-495_988-492dup