Canonical Allele Identifier: CA1519916909
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186195933_186195937delinsGTATT , CM000666.2:g.186195933_186195937delinsGTATT GRCh38
NC_000004.11:g.187117087_187117091delinsGTATT , CM000666.1:g.187117087_187117091delinsGTATT GRCh37
NC_000004.10:g.187354081_187354085delinsGTATT NCBI36
NG_007965.1:g.9414_9418delinsGTATT

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.328-70_328-66delinsGTATT MANE Select ENSP00000368079.4:n.328-70_328-66delinsGT...
ENST00000378802.4:c.328-70_328-66delinsGTATT ENSP00000368079.4:n.328-70_328-66delinsGT...
NM_207352.3:c.328-70_328-66delinsGTATT NP_997235.3:n.328-70_328-66delinsGTATT
XM_005262935.2:c.328-70_328-66delinsGTATT XP_005262992.1:n.328-70_328-66delinsGTATT...
XM_006714184.2:c.18-1007_18-1003delinsGTATT XP_006714247.1:n.18-1007_18-1003delinsGTA...
XM_005262935.4:c.328-70_328-66delinsGTATT XP_005262992.1:n.328-70_328-66delinsGTATT...
XM_017008037.1:c.18-1007_18-1003delinsGTATT XP_016863526.1:n.18-1007_18-1003delinsGTA...
NM_207352.4:c.328-70_328-66delinsGTATT MANE Select NP_997235.3:n.328-70_328-66delinsGTATT
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