Canonical Allele Identifier: CA1980940001
Gene: FADD HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.70206087C= , CM000673.2:g.70206087C= GRCh38
NC_000011.9:g.70052193C= , CM000673.1:g.70052193C= GRCh37
NC_000011.8:g.69729841C= NCBI36
NG_027966.1:g.7925C= , LRG_228:g.7925C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301838.5:c.287-46C= MANE Select ENSP00000301838.5:n.287-46C=
ENST00000301838.4:c.287-46C= ENSP00000301838.4:n.287-46C=
NM_003824.3:c.287-46C= , LRG_228t1:c.287-46C= NP_003815.1:n.287-46C=
NM_003824.4:c.287-46C= MANE Select NP_003815.1:n.287-46C=
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