Canonical Allele Identifier: CA1519920377

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198831_186198834delinsTTAG , CM000666.2:g.186198831_186198834delinsTTAG	GRCh38
NC_000004.11:g.187119985_187119988delinsTTAG , CM000666.1:g.187119985_187119988delinsTTAG	GRCh37
NC_000004.10:g.187356979_187356982delinsTTAG	NCBI36
NG_007965.1:g.12312_12315delinsTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.675-126_675-123delinsTTAG MANE Select	ENSP00000368079.4:n.675-126_675-123delinsTTAG
ENST00000378802.4:c.675-126_675-123delinsTTAG	ENSP00000368079.4:n.675-126_675-123delinsTTAG
ENST00000507209.5:n.1516-126_1516-123delinsTTAG
NM_207352.3:c.675-126_675-123delinsTTAG	NP_997235.3:n.675-126_675-123delinsTTAG
XM_005262935.2:c.675-126_675-123delinsTTAG	XP_005262992.1:n.675-126_675-123delinsTTAG
XM_006714184.2:c.279-126_279-123delinsTTAG	XP_006714247.1:n.279-126_279-123delinsTTAG
XM_005262935.4:c.675-126_675-123delinsTTAG	XP_005262992.1:n.675-126_675-123delinsTTAG
XM_017008037.1:c.279-126_279-123delinsTTAG	XP_016863526.1:n.279-126_279-123delinsTTAG
NM_207352.4:c.675-126_675-123delinsTTAG MANE Select	NP_997235.3:n.675-126_675-123delinsTTAG