Canonical Allele Identifier: CA2764868090
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197764_186197765insAGAC , CM000666.2:g.186197764_186197765insAGAC GRCh38
NC_000004.11:g.187118918_187118919insAGAC , CM000666.1:g.187118918_187118919insAGAC GRCh37
NC_000004.10:g.187355912_187355913insAGAC NCBI36
NG_007965.1:g.11245_11246insAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.674+162_674+163insAGAC MANE Select ENSP00000368079.4:n.674+162_674+163insAGAC
ENST00000378802.4:c.674+162_674+163insAGAC ENSP00000368079.4:n.674+162_674+163insAGAC
ENST00000507209.5:n.1515+162_1515+163insAGAC
NM_207352.3:c.674+162_674+163insAGAC NP_997235.3:n.674+162_674+163insAGAC
XM_005262935.2:c.674+162_674+163insAGAC XP_005262992.1:n.674+162_674+163insAGAC
XM_006714184.2:c.278+162_278+163insAGAC XP_006714247.1:n.278+162_278+163insAGAC
XM_005262935.4:c.674+162_674+163insAGAC XP_005262992.1:n.674+162_674+163insAGAC
XM_017008037.1:c.278+162_278+163insAGAC XP_016863526.1:n.278+162_278+163insAGAC
NM_207352.4:c.674+162_674+163insAGAC MANE Select NP_997235.3:n.674+162_674+163insAGAC