Canonical Allele Identifier: CA2474175083
Gene: FAAH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413715_46413716delinsGA , CM000663.2:g.46413715_46413716delinsGA GRCh38
NC_000001.10:g.46879387_46879388delinsGA , CM000663.1:g.46879387_46879388delinsGA GRCh37
NC_000001.9:g.46651974_46651975delinsGA NCBI36
NG_012195.1:g.24449_24450delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000243167.9:c.*140_*141delinsGA MANE Select ENSP00000243167.8:n.*140_*141delinsGA
ENST00000243167.8:c.*140_*141delinsGA ENSP00000243167.8:n.*140_*141delinsGA
ENST00000484697.5:c.913_914delinsGA
NM_001441.2:c.*140_*141delinsGA NP_001432.2:n.*140_*141delinsGA
NM_001441.3:c.*140_*141delinsGA MANE Select NP_001432.2:n.*140_*141delinsGA
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