Canonical Allele Identifier: CA381665927
Gene: FADD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.70206161T>A , CM000673.2:g.70206161T>A GRCh38
NC_000011.9:g.70052267T>A , CM000673.1:g.70052267T>A GRCh37
NC_000011.8:g.69729915T>A NCBI36
NG_027966.1:g.7999T>A , LRG_228:g.7999T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301838.5:c.315T>A MANE Select ENSP00000301838.5:p.Cys105Ter
ENST00000301838.4:c.315T>A ENSP00000301838.4:p.Cys105Ter
NM_003824.3:c.315T>A , LRG_228t1:c.315T>A NP_003815.1:p.Cys105Ter
NM_003824.4:c.315T>A MANE Select NP_003815.1:p.Cys105Ter