Canonical Allele Identifier: CA2672896843
Gene: CYP4V2 HGNC NCBI

Linked Data

gnomAD v4: 4-186205127-AAG-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.186205130_186205131del , CM000666.2:g.186205130_186205131del GRCh38
NC_000004.11:g.187126284_187126285del , CM000666.1:g.187126284_187126285del GRCh37
NC_000004.10:g.187363278_187363279del NCBI36
NG_007965.1:g.18611_18612del
NG_012095.2:g.1152_1153del

Transcript Alleles

HGVS Amino-acid change
ENST00000378802.5:c.988-70_988-69del MANE Select ENSP00000368079.4:n.988-70_988-69del
ENST00000378802.4:c.988-70_988-69del ENSP00000368079.4:n.988-70_988-69del
ENST00000502665.1:n.223-70_223-69del
ENST00000507209.5:n.5616_5617del
ENST00000513354.5:n.78-70_78-69del
NM_207352.3:c.988-70_988-69del NP_997235.3:n.988-70_988-69del
XM_005262935.2:c.988-70_988-69del XP_005262992.1:n.988-70_988-69del
XM_006714184.2:c.592-70_592-69del XP_006714247.1:n.592-70_592-69del
XM_005262935.4:c.988-70_988-69del XP_005262992.1:n.988-70_988-69del
XM_017008037.1:c.592-70_592-69del XP_016863526.1:n.592-70_592-69del
NM_207352.4:c.988-70_988-69del MANE Select NP_997235.3:n.988-70_988-69del
Search 100 bp 5'
Search 100 bp 3'