Canonical Allele Identifier: CA1519914843
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194428_186194429delinsAC , CM000666.2:g.186194428_186194429delinsAC GRCh38
NC_000004.11:g.187115582_187115583delinsAC , CM000666.1:g.187115582_187115583delinsAC GRCh37
NC_000004.10:g.187352576_187352577delinsAC NCBI36
NG_007965.1:g.7909_7910delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.215-72_215-71delinsAC MANE Select ENSP00000368079.4:n.215-72_215-71delinsAC...
ENST00000378802.4:c.215-72_215-71delinsAC ENSP00000368079.4:n.215-72_215-71delinsAC...
NM_207352.3:c.215-72_215-71delinsAC NP_997235.3:n.215-72_215-71delinsAC
XM_005262935.2:c.215-72_215-71delinsAC XP_005262992.1:n.215-72_215-71delinsAC
XM_005262935.4:c.215-72_215-71delinsAC XP_005262992.1:n.215-72_215-71delinsAC
XM_017008037.1:c.-96-72_-96-71delinsAC XP_016863526.1:n.-96-72_-96-71delinsAC
NM_207352.4:c.215-72_215-71delinsAC MANE Select NP_997235.3:n.215-72_215-71delinsAC