Canonical Allele Identifier: CA382274853
Gene: CASP5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.105007100T>C , CM000673.2:g.105007100T>C GRCh38
NC_000011.9:g.104877827T>C , CM000673.1:g.104877827T>C GRCh37
NC_000011.8:g.104383037T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260315.8:c.416A>G MANE Select ENSP00000260315.3:p.Lys139Arg
ENST00000260315.7:c.416A>G ENSP00000260315.3:p.Lys139Arg
ENST00000393141.6:c.455A>G ENSP00000376849.2:p.Lys152Arg
ENST00000418434.5:c.8-3717A>G ENSP00000398130.1:n.8-3717A>G
ENST00000444749.6:c.242A>G ENSP00000388365.2:p.Lys81Arg
ENST00000456094.1:c.368A>G ENSP00000415241.1:p.Lys123Arg
ENST00000456200.5:c.242A>G ENSP00000408455.1:p.Lys81Arg
ENST00000526056.5:c.455A>G ENSP00000436877.1:p.Lys152Arg
ENST00000531367.5:c.8-3717A>G ENSP00000434471.1:n.8-3717A>G
NM_001136109.1:c.242A>G NP_001129581.1:p.Lys81Arg
NM_001136110.1:c.8-3717A>G NP_001129582.1:n.8-3717A>G
NM_001136112.1:c.455A>G NP_001129584.1:p.Lys152Arg
NM_004347.3:c.416A>G NP_004338.3:p.Lys139Arg
NR_024239.1:n.274A>G
NR_036562.1:n.40-4899A>G
XM_011543020.1:c.181+1707A>G XP_011541322.1:n.181+1707A>G
XM_011543021.1:c.416A>G XP_011541323.1:p.Lys139Arg
NM_001136109.2:c.242A>G NP_001129581.1:p.Lys81Arg
NM_001136110.2:c.8-3717A>G NP_001129582.1:n.8-3717A>G
NM_001136112.2:c.455A>G NP_001129584.1:p.Lys152Arg
NM_004347.4:c.416A>G NP_004338.3:p.Lys139Arg
NR_024239.2:n.274A>G
NR_036562.2:n.40-4899A>G
XM_011543021.2:c.416A>G XP_011541323.1:p.Lys139Arg
NM_004347.5:c.416A>G MANE Select NP_004338.3:p.Lys139Arg
NM_001136109.3:c.242A>G NP_001129581.1:p.Lys81Arg
NM_001136110.3:c.8-3717A>G NP_001129582.1:n.8-3717A>G
NM_001136112.3:c.455A>G NP_001129584.1:p.Lys152Arg
NR_024239.3:n.274A>G
NR_036562.3:n.40-4899A>G