Canonical Allele Identifier: CA792327654

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1213239424
• MyVariant Identifiers: chr4:g.187129842_187129852del (hg19) ; chr4:g.186208688_186208698del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208697_186208707del , CM000666.2:g.186208697_186208707del	GRCh38
NC_000004.11:g.187129851_187129861del , CM000666.1:g.187129851_187129861del	GRCh37
NC_000004.10:g.187366845_187366855del	NCBI36
NG_007965.1:g.22178_22188del
NG_012095.2:g.4719_4729del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-168_1091-158del MANE Select	ENSP00000368079.4:n.1091-168_1091-158del
ENST00000378802.4:c.1091-168_1091-158del	ENSP00000368079.4:n.1091-168_1091-158del
ENST00000502665.1:n.326-168_326-158del
ENST00000507209.5:n.5789-168_5789-158del
ENST00000513354.5:n.181-168_181-158del
NM_207352.3:c.1091-168_1091-158del	NP_997235.3:n.1091-168_1091-158del
XM_005262935.2:c.1091-168_1091-158del	XP_005262992.1:n.1091-168_1091-158del
XM_006714184.2:c.695-168_695-158del	XP_006714247.1:n.695-168_695-158del
XM_005262935.4:c.1091-168_1091-158del	XP_005262992.1:n.1091-168_1091-158del
XM_017008037.1:c.695-168_695-158del	XP_016863526.1:n.695-168_695-158del
NM_207352.4:c.1091-168_1091-158del MANE Select	NP_997235.3:n.1091-168_1091-158del