Canonical Allele Identifier: CA2672895970

Gene: CYP4V2

Linked Data

• gnomAD v4: 4-186204638-TGTAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204640_186204644del , CM000666.2:g.186204640_186204644del	GRCh38
NC_000004.11:g.187125794_187125798del , CM000666.1:g.187125794_187125798del	GRCh37
NC_000004.10:g.187362788_187362792del	NCBI36
NG_007965.1:g.18121_18125del
NG_012095.2:g.662_666del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-560_988-556del MANE Select	ENSP00000368079.4:n.988-560_988-556del
ENST00000378802.4:c.988-560_988-556del	ENSP00000368079.4:n.988-560_988-556del
ENST00000507209.5:n.5126_5130del
ENST00000513354.5:n.77+183_77+187del
NM_207352.3:c.988-560_988-556del	NP_997235.3:n.988-560_988-556del
XM_005262935.2:c.988-560_988-556del	XP_005262992.1:n.988-560_988-556del
XM_006714184.2:c.592-560_592-556del	XP_006714247.1:n.592-560_592-556del
XM_005262935.4:c.988-560_988-556del	XP_005262992.1:n.988-560_988-556del
XM_017008037.1:c.592-560_592-556del	XP_016863526.1:n.592-560_592-556del
NM_207352.4:c.988-560_988-556del MANE Select	NP_997235.3:n.988-560_988-556del