Canonical Allele Identifier: CA1320996995

Gene: CASP8 FLACC1

Genomic Alleles

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

Transcript Alleles

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