Canonical Allele Identifier: CA2645461834
Gene: FAAH HGNC NCBI

Linked Data

gnomAD v4: 1-46413717-AGCGCC-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.46413719_46413723del , CM000663.2:g.46413719_46413723del GRCh38
NC_000001.10:g.46879391_46879395del , CM000663.1:g.46879391_46879395del GRCh37
NC_000001.9:g.46651978_46651982del NCBI36
NG_012195.1:g.24453_24457del

Transcript Alleles

HGVS Amino-acid Change
ENST00000243167.9:c.*144_*148del MANE Select ENSP00000243167.8:n.*144_*148del
ENST00000243167.8:c.*144_*148del ENSP00000243167.8:n.*144_*148del
ENST00000484697.5:c.917_921del
NM_001441.2:c.*144_*148del NP_001432.2:n.*144_*148del
NM_001441.3:c.*144_*148del MANE Select NP_001432.2:n.*144_*148del
Search 100 bp 5'
Search 100 bp 3'