Canonical Allele Identifier: CA2672897277
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186208812-A-AC
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186208817dup , CM000666.2:g.186208817dup GRCh38
NC_000004.11:g.187129971dup , CM000666.1:g.187129971dup GRCh37
NC_000004.10:g.187366965dup NCBI36
NG_007965.1:g.22298dup
NG_012095.2:g.4839dup

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.1091-48dup MANE Select ENSP00000368079.4:n.1091-48dup
ENST00000378802.4:c.1091-48dup ENSP00000368079.4:n.1091-48dup
ENST00000502665.1:n.326-48dup
ENST00000507209.5:n.5789-48dup
ENST00000513354.5:n.181-48dup
NM_207352.3:c.1091-48dup NP_997235.3:n.1091-48dup
XM_005262935.2:c.1091-48dup XP_005262992.1:n.1091-48dup
XM_006714184.2:c.695-48dup XP_006714247.1:n.695-48dup
XM_005262935.4:c.1091-48dup XP_005262992.1:n.1091-48dup
XM_017008037.1:c.695-48dup XP_016863526.1:n.695-48dup
NM_207352.4:c.1091-48dup MANE Select NP_997235.3:n.1091-48dup
Search 100 bp 5'
Search 100 bp 3'