Canonical Allele Identifier: CA382274870

Gene: CASP5

Linked Data

• gnomAD v4: 11-105007103-T-C
• MyVariant Identifiers: chr11:g.104877830T>C (hg19) ; chr11:g.105007103T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105007103T>C , CM000673.2:g.105007103T>C	GRCh38
NC_000011.9:g.104877830T>C , CM000673.1:g.104877830T>C	GRCh37
NC_000011.8:g.104383040T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260315.8:c.413A>G MANE Select	ENSP00000260315.3:p.Gln138Arg
ENST00000260315.7:c.413A>G	ENSP00000260315.3:p.Gln138Arg
ENST00000393141.6:c.452A>G	ENSP00000376849.2:p.Gln151Arg
ENST00000418434.5:c.8-3720A>G	ENSP00000398130.1:n.8-3720A>G
ENST00000444749.6:c.239A>G	ENSP00000388365.2:p.Gln80Arg
ENST00000456094.1:c.365A>G	ENSP00000415241.1:p.Gln122Arg
ENST00000456200.5:c.239A>G	ENSP00000408455.1:p.Gln80Arg
ENST00000526056.5:c.452A>G	ENSP00000436877.1:p.Gln151Arg
ENST00000531367.5:c.8-3720A>G	ENSP00000434471.1:n.8-3720A>G
NM_001136109.1:c.239A>G	NP_001129581.1:p.Gln80Arg
NM_001136110.1:c.8-3720A>G	NP_001129582.1:n.8-3720A>G
NM_001136112.1:c.452A>G	NP_001129584.1:p.Gln151Arg
NM_004347.3:c.413A>G	NP_004338.3:p.Gln138Arg
NR_024239.1:n.271A>G
NR_036562.1:n.40-4902A>G
XM_011543020.1:c.181+1704A>G	XP_011541322.1:n.181+1704A>G
XM_011543021.1:c.413A>G	XP_011541323.1:p.Gln138Arg
NM_001136109.2:c.239A>G	NP_001129581.1:p.Gln80Arg
NM_001136110.2:c.8-3720A>G	NP_001129582.1:n.8-3720A>G
NM_001136112.2:c.452A>G	NP_001129584.1:p.Gln151Arg
NM_004347.4:c.413A>G	NP_004338.3:p.Gln138Arg
NR_024239.2:n.271A>G
NR_036562.2:n.40-4902A>G
XM_011543021.2:c.413A>G	XP_011541323.1:p.Gln138Arg
NM_004347.5:c.413A>G MANE Select	NP_004338.3:p.Gln138Arg
NM_001136109.3:c.239A>G	NP_001129581.1:p.Gln80Arg
NM_001136110.3:c.8-3720A>G	NP_001129582.1:n.8-3720A>G
NM_001136112.3:c.452A>G	NP_001129584.1:p.Gln151Arg
NR_024239.3:n.271A>G
NR_036562.3:n.40-4902A>G