Canonical Allele Identifier: CA15195618

Gene: CASP8 FLACC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201298088A>G , CM000664.2:g.201298088A>G	GRCh38
NC_000002.11:g.202162811A>G , CM000664.1:g.202162811A>G	GRCh37
NC_000002.10:g.201871056A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000696069.1:c.1259+12771A>G (CASP8)	ENSP00000512371.1:n.1259+12771A>G
ENST00000392257.8:c.942+1150T>C (FLACC1) MANE Select	ENSP00000376086.3:n.942+1150T>C
ENST00000286190.9:c.942+1150T>C (FLACC1)	ENSP00000286190.5:n.942+1150T>C
ENST00000392257.7:c.942+1150T>C (FLACC1)	ENSP00000376086.3:n.942+1150T>C
ENST00000405148.6:c.942+1150T>C (FLACC1)	ENSP00000385098.2:n.942+1150T>C
ENST00000415745.5:c.266+1150T>C (FLACC1)
ENST00000439709.5:c.942+1150T>C (FLACC1)	ENSP00000412073.1:n.942+1150T>C
ENST00000494171.5:n.1444+1150T>C (FLACC1)
NM_001127391.2:c.942+1150T>C (FLACC1)	NP_001120863.1:n.942+1150T>C
NM_001289993.1:c.942+1150T>C (FLACC1)	NP_001276922.1:n.942+1150T>C
NM_139163.3:c.942+1150T>C (FLACC1)	NP_631902.2:n.942+1150T>C
NR_110620.1:n.1498+1150T>C (FLACC1)
XM_011510606.1:c.942+1150T>C (FLACC1)	XP_011508908.1:n.942+1150T>C
XM_011510607.1:c.942+1150T>C (FLACC1)	XP_011508909.1:n.942+1150T>C
XM_011510608.1:c.942+1150T>C (FLACC1)	XP_011508910.1:n.942+1150T>C
XM_011510609.1:c.942+1150T>C (FLACC1)	XP_011508911.1:n.942+1150T>C
XM_011510610.1:c.633+1150T>C (FLACC1)	XP_011508912.1:n.633+1150T>C
XM_011510611.1:c.942+1150T>C (FLACC1)	XP_011508913.1:n.942+1150T>C
XM_011510612.1:c.315+1150T>C (FLACC1)	XP_011508914.1:n.315+1150T>C
XM_011510606.3:c.942+1150T>C (FLACC1)	XP_011508908.1:n.942+1150T>C
XM_011510610.3:c.633+1150T>C (FLACC1)	XP_011508912.1:n.633+1150T>C
XM_011510612.3:c.315+1150T>C (FLACC1)	XP_011508914.1:n.315+1150T>C
XM_017003361.2:c.942+1150T>C (FLACC1)	XP_016858850.1:n.942+1150T>C
XM_017003362.2:c.315+1150T>C (FLACC1)	XP_016858851.1:n.315+1150T>C
XM_024452696.1:c.942+1150T>C (FLACC1)	XP_024308464.1:n.942+1150T>C
XM_024452697.1:c.942+1150T>C (FLACC1)	XP_024308465.1:n.942+1150T>C
NM_001127391.3:c.942+1150T>C (FLACC1) MANE Select	NP_001120863.1:n.942+1150T>C
NM_001289993.2:c.942+1150T>C (FLACC1)	NP_001276922.1:n.942+1150T>C
NR_110620.2:n.1445+1150T>C (FLACC1)
NM_139163.4:c.942+1150T>C (FLACC1)	NP_631902.2:n.942+1150T>C