Canonical Allele Identifier: CA1519914980
Gene: CYP4V2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186194516_186194519delinsCATT , CM000666.2:g.186194516_186194519delinsCATT GRCh38
NC_000004.11:g.187115670_187115673delinsCATT , CM000666.1:g.187115670_187115673delinsCATT GRCh37
NC_000004.10:g.187352664_187352667delinsCATT NCBI36
NG_007965.1:g.7997_8000delinsCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378802.5:c.231_234delinsCATT MANE Select ENSP00000368079.4:p.Ile77=
ENST00000378802.4:c.231_234delinsCATT ENSP00000368079.4:p.Ile77=
NM_207352.3:c.231_234delinsCATT NP_997235.3:p.Ile77=
XM_005262935.2:c.231_234delinsCATT XP_005262992.1:p.Ile77=
XM_005262935.4:c.231_234delinsCATT XP_005262992.1:p.Ile77=
XM_017008037.1:c.-80_-77delinsCATT XP_016863526.1:n.-80_-77delinsCATT
NM_207352.4:c.231_234delinsCATT MANE Select NP_997235.3:p.Ile77=
Search 100 bp 5'
Search 100 bp 3'