Canonical Allele Identifier: CA601247888

Gene: CASP5

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105004534T>A , CM000673.2:g.105004534T>A	GRCh38
NC_000011.9:g.104875261T>A , CM000673.1:g.104875261T>A	GRCh37
NC_000011.8:g.104380471T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260315.8:c.434-1151A>T MANE Select	ENSP00000260315.3:n.434-1151A>T
ENST00000260315.7:c.434-1151A>T	ENSP00000260315.3:n.434-1151A>T
ENST00000393141.6:c.473-1151A>T	ENSP00000376849.2:n.473-1151A>T
ENST00000418434.5:c.8-1151A>T	ENSP00000398130.1:n.8-1151A>T
ENST00000444749.6:c.260-1151A>T	ENSP00000388365.2:n.260-1151A>T
ENST00000456094.1:c.386-1151A>T	ENSP00000415241.1:n.386-1151A>T
ENST00000456200.5:c.260-2333A>T	ENSP00000408455.1:n.260-2333A>T
ENST00000526056.5:c.473-1151A>T	ENSP00000436877.1:n.473-1151A>T
ENST00000531367.5:c.8-1151A>T	ENSP00000434471.1:n.8-1151A>T
NM_001136109.1:c.260-1151A>T	NP_001129581.1:n.260-1151A>T
NM_001136110.1:c.8-1151A>T	NP_001129582.1:n.8-1151A>T
NM_001136112.1:c.473-1151A>T	NP_001129584.1:n.473-1151A>T
NM_004347.3:c.434-1151A>T	NP_004338.3:n.434-1151A>T
NR_024239.1:n.292-2333A>T
NR_036562.1:n.40-2333A>T
XM_011543020.1:c.182-1151A>T	XP_011541322.1:n.182-1151A>T
XM_011543021.1:c.434-1151A>T	XP_011541323.1:n.434-1151A>T
NM_001136109.2:c.260-1151A>T	NP_001129581.1:n.260-1151A>T
NM_001136110.2:c.8-1151A>T	NP_001129582.1:n.8-1151A>T
NM_001136112.2:c.473-1151A>T	NP_001129584.1:n.473-1151A>T
NM_004347.4:c.434-1151A>T	NP_004338.3:n.434-1151A>T
NR_024239.2:n.292-2333A>T
NR_036562.2:n.40-2333A>T
XM_011543021.2:c.434-1151A>T	XP_011541323.1:n.434-1151A>T
NM_004347.5:c.434-1151A>T MANE Select	NP_004338.3:n.434-1151A>T
NM_001136109.3:c.260-1151A>T	NP_001129581.1:n.260-1151A>T
NM_001136110.3:c.8-1151A>T	NP_001129582.1:n.8-1151A>T
NM_001136112.3:c.473-1151A>T	NP_001129584.1:n.473-1151A>T
NR_024239.3:n.292-2333A>T
NR_036562.3:n.40-2333A>T