Canonical Allele Identifier: CA792327736

Gene: CYP4V2

Linked Data

• dbSNP Id: rs780703259
• gnomAD v3: 4-186208819-G-GC
• gnomAD v4: 4-186208819-G-GC
• MyVariant Identifiers: chr4:g.187129973_187129974insC (hg19) ; chr4:g.186208819_186208820insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208824dup , CM000666.2:g.186208824dup	GRCh38
NC_000004.11:g.187129978dup , CM000666.1:g.187129978dup	GRCh37
NC_000004.10:g.187366972dup	NCBI36
NG_007965.1:g.22305dup
NG_012095.2:g.4846dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.1091-41dup MANE Select	ENSP00000368079.4:n.1091-41dup
ENST00000378802.4:c.1091-41dup	ENSP00000368079.4:n.1091-41dup
ENST00000502665.1:n.326-41dup
ENST00000507209.5:n.5789-41dup
ENST00000513354.5:n.181-41dup
NM_207352.3:c.1091-41dup	NP_997235.3:n.1091-41dup
XM_005262935.2:c.1091-41dup	XP_005262992.1:n.1091-41dup
XM_006714184.2:c.695-41dup	XP_006714247.1:n.695-41dup
XM_005262935.4:c.1091-41dup	XP_005262992.1:n.1091-41dup
XM_017008037.1:c.695-41dup	XP_016863526.1:n.695-41dup
NM_207352.4:c.1091-41dup MANE Select	NP_997235.3:n.1091-41dup