Canonical Allele Identifier: CA792325144

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1425566253
• gnomAD v3: 4-186204831-CAGAT-C
• gnomAD v4: 4-186204831-CAGAT-C
• MyVariant Identifiers: chr4:g.187125986_187125989del (hg19) ; chr4:g.186204832_186204835del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186204832_186204835del , CM000666.2:g.186204832_186204835del	GRCh38
NC_000004.11:g.187125986_187125989del , CM000666.1:g.187125986_187125989del	GRCh37
NC_000004.10:g.187362980_187362983del	NCBI36
NG_007965.1:g.18313_18316del
NG_012095.2:g.854_857del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.988-368_988-365del MANE Select	ENSP00000368079.4:n.988-368_988-365del
ENST00000378802.4:c.988-368_988-365del	ENSP00000368079.4:n.988-368_988-365del
ENST00000507209.5:n.5318_5321del
ENST00000513354.5:n.78-368_78-365del
NM_207352.3:c.988-368_988-365del	NP_997235.3:n.988-368_988-365del
XM_005262935.2:c.988-368_988-365del	XP_005262992.1:n.988-368_988-365del
XM_006714184.2:c.592-368_592-365del	XP_006714247.1:n.592-368_592-365del
XM_005262935.4:c.988-368_988-365del	XP_005262992.1:n.988-368_988-365del
XM_017008037.1:c.592-368_592-365del	XP_016863526.1:n.592-368_592-365del
NM_207352.4:c.988-368_988-365del MANE Select	NP_997235.3:n.988-368_988-365del