Canonical Allele Identifier: CA1519883995

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186200803_186200806delinsTATA , CM000666.2:g.186200803_186200806delinsTATA	GRCh38
NC_000004.11:g.187121957_187121960delinsTATA , CM000666.1:g.187121957_187121960delinsTATA	GRCh37
NC_000004.10:g.187358951_187358954delinsTATA	NCBI36
NG_007965.1:g.14284_14287delinsTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.802-354_802-351delinsTATA MANE Select	ENSP00000368079.4:n.802-354_802-351delinsTATA
ENST00000378802.4:c.802-354_802-351delinsTATA	ENSP00000368079.4:n.802-354_802-351delinsTATA
ENST00000507209.5:n.1643-354_1643-351delinsTATA
NM_207352.3:c.802-354_802-351delinsTATA	NP_997235.3:n.802-354_802-351delinsTATA
XM_005262935.2:c.802-354_802-351delinsTATA	XP_005262992.1:n.802-354_802-351delinsTATA
XM_006714184.2:c.406-354_406-351delinsTATA	XP_006714247.1:n.406-354_406-351delinsTATA
XM_005262935.4:c.802-354_802-351delinsTATA	XP_005262992.1:n.802-354_802-351delinsTATA
XM_017008037.1:c.406-354_406-351delinsTATA	XP_016863526.1:n.406-354_406-351delinsTATA
NM_207352.4:c.802-354_802-351delinsTATA MANE Select	NP_997235.3:n.802-354_802-351delinsTATA