Canonical Allele Identifier: CA381665930
Gene: FADD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.70206163A>C , CM000673.2:g.70206163A>C GRCh38
NC_000011.9:g.70052269A>C , CM000673.1:g.70052269A>C GRCh37
NC_000011.8:g.69729917A>C NCBI36
NG_027966.1:g.8001A>C , LRG_228:g.8001A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000301838.5:c.317A>C MANE Select ENSP00000301838.5:p.Asp106Ala
ENST00000301838.4:c.317A>C ENSP00000301838.4:p.Asp106Ala
NM_003824.3:c.317A>C , LRG_228t1:c.317A>C NP_003815.1:p.Asp106Ala
NM_003824.4:c.317A>C MANE Select NP_003815.1:p.Asp106Ala