Canonical Allele Identifier: CA227444205
Gene: CASP5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.105004030G>A , CM000673.2:g.105004030G>A GRCh38
NC_000011.9:g.104874757G>A , CM000673.1:g.104874757G>A GRCh37
NC_000011.8:g.104379967G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000260315.8:c.434-647C>T MANE Select ENSP00000260315.3:n.434-647C>T
ENST00000260315.7:c.434-647C>T ENSP00000260315.3:n.434-647C>T
ENST00000393141.6:c.473-647C>T ENSP00000376849.2:n.473-647C>T
ENST00000418434.5:c.8-647C>T ENSP00000398130.1:n.8-647C>T
ENST00000444749.6:c.260-647C>T ENSP00000388365.2:n.260-647C>T
ENST00000456094.1:c.386-647C>T ENSP00000415241.1:n.386-647C>T
ENST00000456200.5:c.260-1829C>T ENSP00000408455.1:n.260-1829C>T
ENST00000526056.5:c.473-647C>T ENSP00000436877.1:n.473-647C>T
ENST00000531367.5:c.8-647C>T ENSP00000434471.1:n.8-647C>T
NM_001136109.1:c.260-647C>T NP_001129581.1:n.260-647C>T
NM_001136110.1:c.8-647C>T NP_001129582.1:n.8-647C>T
NM_001136112.1:c.473-647C>T NP_001129584.1:n.473-647C>T
NM_004347.3:c.434-647C>T NP_004338.3:n.434-647C>T
NR_024239.1:n.292-1829C>T
NR_036562.1:n.40-1829C>T
XM_011543020.1:c.182-647C>T XP_011541322.1:n.182-647C>T
XM_011543021.1:c.434-647C>T XP_011541323.1:n.434-647C>T
NM_001136109.2:c.260-647C>T NP_001129581.1:n.260-647C>T
NM_001136110.2:c.8-647C>T NP_001129582.1:n.8-647C>T
NM_001136112.2:c.473-647C>T NP_001129584.1:n.473-647C>T
NM_004347.4:c.434-647C>T NP_004338.3:n.434-647C>T
NR_024239.2:n.292-1829C>T
NR_036562.2:n.40-1829C>T
XM_011543021.2:c.434-647C>T XP_011541323.1:n.434-647C>T
NM_004347.5:c.434-647C>T MANE Select NP_004338.3:n.434-647C>T
NM_001136109.3:c.260-647C>T NP_001129581.1:n.260-647C>T
NM_001136110.3:c.8-647C>T NP_001129582.1:n.8-647C>T
NM_001136112.3:c.473-647C>T NP_001129584.1:n.473-647C>T
NR_024239.3:n.292-1829C>T
NR_036562.3:n.40-1829C>T
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