Canonical Allele Identifier: CA2672897368
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186197319-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186197321del , CM000666.2:g.186197321del GRCh38
NC_000004.11:g.187118475del , CM000666.1:g.187118475del GRCh37
NC_000004.10:g.187355469del NCBI36
NG_007965.1:g.10802del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.604+191del MANE Select ENSP00000368079.4:n.604+191del
ENST00000378802.4:c.604+191del ENSP00000368079.4:n.604+191del
ENST00000507209.5:n.1234del
NM_207352.3:c.604+191del NP_997235.3:n.604+191del
XM_005262935.2:c.604+191del XP_005262992.1:n.604+191del
XM_006714184.2:c.208+191del XP_006714247.1:n.208+191del
XM_005262935.4:c.604+191del XP_005262992.1:n.604+191del
XM_017008037.1:c.208+191del XP_016863526.1:n.208+191del
NM_207352.4:c.604+191del MANE Select NP_997235.3:n.604+191del
Search 100 bp 5'
Search 100 bp 3'