Canonical Allele Identifier: CA381665865

Gene: FADD

Linked Data

• MyVariant Identifiers: chr11:g.70052238G>T (hg19) ; chr11:g.70206132G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.70206132G>T , CM000673.2:g.70206132G>T	GRCh38
NC_000011.9:g.70052238G>T , CM000673.1:g.70052238G>T	GRCh37
NC_000011.8:g.69729886G>T	NCBI36
NG_027966.1:g.7970G>T , LRG_228:g.7970G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301838.5:c.287-1G>T MANE Select	ENSP00000301838.5:n.287-1G>T
ENST00000301838.4:c.287-1G>T	ENSP00000301838.4:n.287-1G>T
NM_003824.3:c.287-1G>T , LRG_228t1:c.287-1G>T	NP_003815.1:n.287-1G>T
NM_003824.4:c.287-1G>T MANE Select	NP_003815.1:n.287-1G>T