Canonical Allele Identifier: CA792320476

Gene: CYP4V2

Linked Data

• dbSNP Id: rs1167781384
• MyVariant Identifiers: chr4:g.187119907_187119918del (hg19) ; chr4:g.186198753_186198764del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198753_186198764del , CM000666.2:g.186198753_186198764del	GRCh38
NC_000004.11:g.187119907_187119918del , CM000666.1:g.187119907_187119918del	GRCh37
NC_000004.10:g.187356901_187356912del	NCBI36
NG_007965.1:g.12234_12245del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.675-204_675-193del MANE Select	ENSP00000368079.4:n.675-204_675-193del
ENST00000378802.4:c.675-204_675-193del	ENSP00000368079.4:n.675-204_675-193del
ENST00000507209.5:n.1516-204_1516-193del
NM_207352.3:c.675-204_675-193del	NP_997235.3:n.675-204_675-193del
XM_005262935.2:c.675-204_675-193del	XP_005262992.1:n.675-204_675-193del
XM_006714184.2:c.279-204_279-193del	XP_006714247.1:n.279-204_279-193del
XM_005262935.4:c.675-204_675-193del	XP_005262992.1:n.675-204_675-193del
XM_017008037.1:c.279-204_279-193del	XP_016863526.1:n.279-204_279-193del
NM_207352.4:c.675-204_675-193del MANE Select	NP_997235.3:n.675-204_675-193del