Canonical Allele Identifier: CA2615772221

Gene: CASP5

Linked Data

• gnomAD v4: 11-105006983-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105006983A>C , CM000673.2:g.105006983A>C	GRCh38
NC_000011.9:g.104877710A>C , CM000673.1:g.104877710A>C	GRCh37
NC_000011.8:g.104382920A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260315.8:c.433+100T>G MANE Select	ENSP00000260315.3:n.433+100T>G
ENST00000260315.7:c.433+100T>G	ENSP00000260315.3:n.433+100T>G
ENST00000393141.6:c.472+100T>G	ENSP00000376849.2:n.472+100T>G
ENST00000418434.5:c.8-3600T>G	ENSP00000398130.1:n.8-3600T>G
ENST00000444749.6:c.259+100T>G	ENSP00000388365.2:n.259+100T>G
ENST00000456094.1:c.385+100T>G	ENSP00000415241.1:n.385+100T>G
ENST00000456200.5:c.259+100T>G	ENSP00000408455.1:n.259+100T>G
ENST00000526056.5:c.472+100T>G	ENSP00000436877.1:n.472+100T>G
ENST00000531367.5:c.8-3600T>G	ENSP00000434471.1:n.8-3600T>G
NM_001136109.1:c.259+100T>G	NP_001129581.1:n.259+100T>G
NM_001136110.1:c.8-3600T>G	NP_001129582.1:n.8-3600T>G
NM_001136112.1:c.472+100T>G	NP_001129584.1:n.472+100T>G
NM_004347.3:c.433+100T>G	NP_004338.3:n.433+100T>G
NR_024239.1:n.291+100T>G
NR_036562.1:n.40-4782T>G
XM_011543020.1:c.181+1824T>G	XP_011541322.1:n.181+1824T>G
XM_011543021.1:c.433+100T>G	XP_011541323.1:n.433+100T>G
NM_001136109.2:c.259+100T>G	NP_001129581.1:n.259+100T>G
NM_001136110.2:c.8-3600T>G	NP_001129582.1:n.8-3600T>G
NM_001136112.2:c.472+100T>G	NP_001129584.1:n.472+100T>G
NM_004347.4:c.433+100T>G	NP_004338.3:n.433+100T>G
NR_024239.2:n.291+100T>G
NR_036562.2:n.40-4782T>G
XM_011543021.2:c.433+100T>G	XP_011541323.1:n.433+100T>G
NM_004347.5:c.433+100T>G MANE Select	NP_004338.3:n.433+100T>G
NM_001136109.3:c.259+100T>G	NP_001129581.1:n.259+100T>G
NM_001136110.3:c.8-3600T>G	NP_001129582.1:n.8-3600T>G
NM_001136112.3:c.472+100T>G	NP_001129584.1:n.472+100T>G
NR_024239.3:n.291+100T>G
NR_036562.3:n.40-4782T>G