Canonical Allele Identifier: CA2672895337
Gene: CYP4V2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194647_186194648insCA , CM000666.2:g.186194647_186194648insCA GRCh38
NC_000004.11:g.187115801_187115802insCA , CM000666.1:g.187115801_187115802insCA GRCh37
NC_000004.10:g.187352795_187352796insCA NCBI36
NG_007965.1:g.8128_8129insCA

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.327+35_327+36insCA MANE Select ENSP00000368079.4:n.327+35_327+36insCA
ENST00000378802.4:c.327+35_327+36insCA ENSP00000368079.4:n.327+35_327+36insCA
NM_207352.3:c.327+35_327+36insCA NP_997235.3:n.327+35_327+36insCA
XM_005262935.2:c.327+35_327+36insCA XP_005262992.1:n.327+35_327+36insCA
XM_006714184.2:c.17+35_17+36insCA XP_006714247.1:n.17+35_17+36insCA
XM_005262935.4:c.327+35_327+36insCA XP_005262992.1:n.327+35_327+36insCA
XM_017008037.1:c.17+35_17+36insCA XP_016863526.1:n.17+35_17+36insCA
NM_207352.4:c.327+35_327+36insCA MANE Select NP_997235.3:n.327+35_327+36insCA