Canonical Allele Identifier: CA1519920368

Gene: CYP4V2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.186198810_186198811delinsTA , CM000666.2:g.186198810_186198811delinsTA	GRCh38
NC_000004.11:g.187119964_187119965delinsTA , CM000666.1:g.187119964_187119965delinsTA	GRCh37
NC_000004.10:g.187356958_187356959delinsTA	NCBI36
NG_007965.1:g.12291_12292delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378802.5:c.675-147_675-146delinsTA MANE Select	ENSP00000368079.4:n.675-147_675-146delinsTA
ENST00000378802.4:c.675-147_675-146delinsTA	ENSP00000368079.4:n.675-147_675-146delinsTA
ENST00000507209.5:n.1516-147_1516-146delinsTA
NM_207352.3:c.675-147_675-146delinsTA	NP_997235.3:n.675-147_675-146delinsTA
XM_005262935.2:c.675-147_675-146delinsTA	XP_005262992.1:n.675-147_675-146delinsTA
XM_006714184.2:c.279-147_279-146delinsTA	XP_006714247.1:n.279-147_279-146delinsTA
XM_005262935.4:c.675-147_675-146delinsTA	XP_005262992.1:n.675-147_675-146delinsTA
XM_017008037.1:c.279-147_279-146delinsTA	XP_016863526.1:n.279-147_279-146delinsTA
NM_207352.4:c.675-147_675-146delinsTA MANE Select	NP_997235.3:n.675-147_675-146delinsTA