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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA358946908
Gene: CYP4V2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr4:g.187115705T>A (hg19)
chr4:g.186194551T>A (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.186194551T>A , CM000666.2:g.186194551T>A
GRCh38
NC_000004.11:g.187115705T>A , CM000666.1:g.187115705T>A
GRCh37
NC_000004.10:g.187352699T>A
NCBI36
NG_007965.1:g.8032T>A
Transcript Alleles
HGVS
Amino-acid change
ENST00000378802.5:c.266T>A
MANE Select
ENSP00000368079.4:p.Leu89Gln
ENST00000378802.4:c.266T>A
ENSP00000368079.4:p.Leu89Gln
NM_207352.3:c.266T>A
NP_997235.3:p.Leu89Gln
XM_005262935.2:c.266T>A
XP_005262992.1:p.Leu89Gln
XM_006714184.2:c.-45T>A
XP_006714247.1:n.-45T>A
XM_005262935.4:c.266T>A
XP_005262992.1:p.Leu89Gln
XM_017008037.1:c.-45T>A
XP_016863526.1:n.-45T>A
NM_207352.4:c.266T>A
MANE Select
NP_997235.3:p.Leu89Gln
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