Canonical Allele Identifier: CA1997261901

Gene: CASP5

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.105008835A= , CM000673.2:g.105008835A=	GRCh38
NC_000011.9:g.104879562A= , CM000673.1:g.104879562A=	GRCh37
NC_000011.8:g.104384772A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_004347.5:c.153T= MANE Select	NP_004338.3:p.Asn51=
ENST00000260315.8:c.153T= MANE Select	ENSP00000260315.3:p.Asn51=
NM_001136109.1:c.8-1501T=	NP_001129581.1:n.8-1501T=
NM_001136109.2:c.8-1501T=	NP_001129581.1:n.8-1501T=
NM_001136109.3:c.8-1501T=	NP_001129581.1:n.8-1501T=
NM_001136110.1:c.8-5452T=	NP_001129582.1:n.8-5452T=
NM_001136110.2:c.8-5452T=	NP_001129582.1:n.8-5452T=
NM_001136110.3:c.8-5452T=	NP_001129582.1:n.8-5452T=
NM_001136112.1:c.192T=	NP_001129584.1:p.Asn64=
NM_001136112.2:c.192T=	NP_001129584.1:p.Asn64=
NM_001136112.3:c.192T=	NP_001129584.1:p.Asn64=
NM_004347.3:c.153T=	NP_004338.3:p.Asn51=
NM_004347.4:c.153T=	NP_004338.3:p.Asn51=
NR_024239.1:n.40-1501T=
NR_024239.2:n.40-1501T=
NR_024239.3:n.40-1501T=
NR_036562.1:n.40-6634T=
NR_036562.2:n.40-6634T=
NR_036562.3:n.40-6634T=
ENST00000260315.7:c.153T=	ENSP00000260315.3:p.Asn51=
ENST00000393141.6:c.192T=	ENSP00000376849.2:p.Asn64=
ENST00000418434.5:c.8-5452T=	ENSP00000398130.1:n.8-5452T=
ENST00000444749.6:c.8-1501T=	ENSP00000388365.2:n.8-1501T=
ENST00000456094.1:c.105T=	ENSP00000415241.1:p.Asn35=
ENST00000456200.5:c.8-1501T=	ENSP00000408455.1:n.8-1501T=
ENST00000526056.5:c.192T=	ENSP00000436877.1:p.Asn64=
ENST00000531367.5:c.8-5452T=	ENSP00000434471.1:n.8-5452T=
XM_011543020.1:c.153T=	XP_011541322.1:p.Asn51=
XM_011543021.1:c.153T=	XP_011541323.1:p.Asn51=
XM_011543021.2:c.153T=	XP_011541323.1:p.Asn51=