Canonical Allele Identifier: CA671102604

Gene: CASP5

Linked Data

• dbSNP Id: rs1192441872
• gnomAD v4: 11-105006981-G-A
• MyVariant Identifiers: chr11:g.104877708G>A (hg19) ; chr11:g.105006981G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105006981G>A , CM000673.2:g.105006981G>A	GRCh38
NC_000011.9:g.104877708G>A , CM000673.1:g.104877708G>A	GRCh37
NC_000011.8:g.104382918G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000260315.8:c.433+102C>T MANE Select	ENSP00000260315.3:n.433+102C>T
ENST00000260315.7:c.433+102C>T	ENSP00000260315.3:n.433+102C>T
ENST00000393141.6:c.472+102C>T	ENSP00000376849.2:n.472+102C>T
ENST00000418434.5:c.8-3598C>T	ENSP00000398130.1:n.8-3598C>T
ENST00000444749.6:c.259+102C>T	ENSP00000388365.2:n.259+102C>T
ENST00000456094.1:c.385+102C>T	ENSP00000415241.1:n.385+102C>T
ENST00000456200.5:c.259+102C>T	ENSP00000408455.1:n.259+102C>T
ENST00000526056.5:c.472+102C>T	ENSP00000436877.1:n.472+102C>T
ENST00000531367.5:c.8-3598C>T	ENSP00000434471.1:n.8-3598C>T
NM_001136109.1:c.259+102C>T	NP_001129581.1:n.259+102C>T
NM_001136110.1:c.8-3598C>T	NP_001129582.1:n.8-3598C>T
NM_001136112.1:c.472+102C>T	NP_001129584.1:n.472+102C>T
NM_004347.3:c.433+102C>T	NP_004338.3:n.433+102C>T
NR_024239.1:n.291+102C>T
NR_036562.1:n.40-4780C>T
XM_011543020.1:c.181+1826C>T	XP_011541322.1:n.181+1826C>T
XM_011543021.1:c.433+102C>T	XP_011541323.1:n.433+102C>T
NM_001136109.2:c.259+102C>T	NP_001129581.1:n.259+102C>T
NM_001136110.2:c.8-3598C>T	NP_001129582.1:n.8-3598C>T
NM_001136112.2:c.472+102C>T	NP_001129584.1:n.472+102C>T
NM_004347.4:c.433+102C>T	NP_004338.3:n.433+102C>T
NR_024239.2:n.291+102C>T
NR_036562.2:n.40-4780C>T
XM_011543021.2:c.433+102C>T	XP_011541323.1:n.433+102C>T
NM_004347.5:c.433+102C>T MANE Select	NP_004338.3:n.433+102C>T
NM_001136109.3:c.259+102C>T	NP_001129581.1:n.259+102C>T
NM_001136110.3:c.8-3598C>T	NP_001129582.1:n.8-3598C>T
NM_001136112.3:c.472+102C>T	NP_001129584.1:n.472+102C>T
NR_024239.3:n.291+102C>T
NR_036562.3:n.40-4780C>T