Canonical Allele Identifier: CA1519915291
Gene: CYP4V2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194637_186194638delinsTA , CM000666.2:g.186194637_186194638delinsTA GRCh38
NC_000004.11:g.187115791_187115792delinsTA , CM000666.1:g.187115791_187115792delinsTA GRCh37
NC_000004.10:g.187352785_187352786delinsTA NCBI36
NG_007965.1:g.8118_8119delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.327+25_327+26delinsTA MANE Select ENSP00000368079.4:n.327+25_327+26delinsTA...
ENST00000378802.4:c.327+25_327+26delinsTA ENSP00000368079.4:n.327+25_327+26delinsTA...
NM_207352.3:c.327+25_327+26delinsTA NP_997235.3:n.327+25_327+26delinsTA
XM_005262935.2:c.327+25_327+26delinsTA XP_005262992.1:n.327+25_327+26delinsTA
XM_006714184.2:c.17+25_17+26delinsTA XP_006714247.1:n.17+25_17+26delinsTA
XM_005262935.4:c.327+25_327+26delinsTA XP_005262992.1:n.327+25_327+26delinsTA
XM_017008037.1:c.17+25_17+26delinsTA XP_016863526.1:n.17+25_17+26delinsTA
NM_207352.4:c.327+25_327+26delinsTA MANE Select NP_997235.3:n.327+25_327+26delinsTA