Canonical Allele Identifier: CA792327688

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1463929322
• MyVariant Identifiers: chr4:g.187129904del (hg19) ; chr4:g.186208750del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186208752del , CM000666.2:g.186208752del	GRCh38
NC_000004.11:g.187129906del , CM000666.1:g.187129906del	GRCh37
NC_000004.10:g.187366900del	NCBI36
NG_007965.1:g.22233del
NG_012095.2:g.4774del

Transcript Alleles

HGVS	Amino-acid change
ENST00000378802.5:c.1091-113del MANE Select	ENSP00000368079.4:n.1091-113del
ENST00000378802.4:c.1091-113del	ENSP00000368079.4:n.1091-113del
ENST00000502665.1:n.326-113del
ENST00000507209.5:n.5789-113del
ENST00000513354.5:n.181-113del
NM_207352.3:c.1091-113del	NP_997235.3:n.1091-113del
XM_005262935.2:c.1091-113del	XP_005262992.1:n.1091-113del
XM_006714184.2:c.695-113del	XP_006714247.1:n.695-113del
XM_005262935.4:c.1091-113del	XP_005262992.1:n.1091-113del
XM_017008037.1:c.695-113del	XP_016863526.1:n.695-113del
NM_207352.4:c.1091-113del MANE Select	NP_997235.3:n.1091-113del