Canonical Allele Identifier: CA2672896534

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204921-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204922dup , CM000666.2:g.186204922dup	GRCh38
NC_000004.11:g.187126076dup , CM000666.1:g.187126076dup	GRCh37
NC_000004.10:g.187363070dup	NCBI36
NG_007965.1:g.18403dup
NG_012095.2:g.944dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-278dup MANE Select	ENSP00000368079.4:n.988-278dup
ENST00000378802.4:c.988-278dup	ENSP00000368079.4:n.988-278dup
ENST00000502665.1:n.86dup
ENST00000507209.5:n.5408dup
ENST00000513354.5:n.78-278dup
NM_207352.3:c.988-278dup	NP_997235.3:n.988-278dup
XM_005262935.2:c.988-278dup	XP_005262992.1:n.988-278dup
XM_006714184.2:c.592-278dup	XP_006714247.1:n.592-278dup
XM_005262935.4:c.988-278dup	XP_005262992.1:n.988-278dup
XM_017008037.1:c.592-278dup	XP_016863526.1:n.592-278dup
NM_207352.4:c.988-278dup MANE Select	NP_997235.3:n.988-278dup