Canonical Allele Identifier: CA792325059

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1163315470
• MyVariant Identifiers: chr4:g.187125757_187125759del (hg19) ; chr4:g.186204603_186204605del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204605_186204607del , CM000666.2:g.186204605_186204607del	GRCh38
NC_000004.11:g.187125759_187125761del , CM000666.1:g.187125759_187125761del	GRCh37
NC_000004.10:g.187362753_187362755del	NCBI36
NG_007965.1:g.18086_18088del
NG_012095.2:g.627_629del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-595_988-593del MANE Select	ENSP00000368079.4:n.988-595_988-593del
ENST00000378802.4:c.988-595_988-593del	ENSP00000368079.4:n.988-595_988-593del
ENST00000507209.5:n.5091_5093del
ENST00000513354.5:n.77+148_77+150del
NM_207352.3:c.988-595_988-593del	NP_997235.3:n.988-595_988-593del
XM_005262935.2:c.988-595_988-593del	XP_005262992.1:n.988-595_988-593del
XM_006714184.2:c.592-595_592-593del	XP_006714247.1:n.592-595_592-593del
XM_005262935.4:c.988-595_988-593del	XP_005262992.1:n.988-595_988-593del
XM_017008037.1:c.592-595_592-593del	XP_016863526.1:n.592-595_592-593del
NM_207352.4:c.988-595_988-593del MANE Select	NP_997235.3:n.988-595_988-593del