Canonical Allele Identifier: CA1320996996

Gene: CASP8 FLACC1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201288355T>A , CM000664.2:g.201288355T>A	GRCh38
NC_000002.11:g.202153078T>A , CM000664.1:g.202153078T>A	GRCh37
NC_000002.10:g.201861323T>A	NCBI36
NG_007497.1:g.59898T>A , LRG_34:g.59898T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+3038T>A (CASP8)	ENSP00000512371.1:n.1259+3038T>A
ENST00000392257.8:c.*300A>T (FLACC1) MANE Select	ENSP00000376086.3:n.*300A>T
ENST00000286190.9:c.*300A>T (FLACC1)	ENSP00000286190.5:n.*300A>T
NM_001127391.2:c.*300A>T (FLACC1)	NP_001120863.1:n.*300A>T
NM_001289993.1:c.*300A>T (FLACC1)	NP_001276922.1:n.*300A>T
NM_139163.3:c.*300A>T (FLACC1)	NP_631902.2:n.*300A>T
NR_110620.1:n.2199A>T (FLACC1)
NM_001127391.3:c.*300A>T (FLACC1) MANE Select	NP_001120863.1:n.*300A>T
NM_001289993.2:c.*300A>T (FLACC1)	NP_001276922.1:n.*300A>T
NR_110620.2:n.2146A>T (FLACC1)
NM_139163.4:c.*300A>T (FLACC1)	NP_631902.2:n.*300A>T