Canonical Allele Identifier: CA2551686925
Gene: CASP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.184628951_184628952insTATTGAGAAAGAAA , CM000666.2:g.184628951_184628952insTATTGAGAAAGAAA GRCh38
NC_000004.11:g.185550105_185550106insTATTGAGAAAGAAA , CM000666.1:g.185550105_185550106insTATTGAGAAAGAAA GRCh37
NC_000004.10:g.185787099_185787100insTATTGAGAAAGAAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000700100.1:c.*322_*323insTCTTTCTCAATATT ENSP00000514797.1:n.*322_*323insTCTTTCTCA...
ENST00000700101.1:c.*322_*323insTCTTTCTCAATATT ENSP00000514798.1:n.*322_*323insTCTTTCTCA...
ENST00000700102.1:n.2759_2760insTCTTTCTCAATATT
ENST00000700103.1:n.4121_4122insTCTTTCTCAATATT
ENST00000700104.1:c.*905_*906insTCTTTCTCAATATT ENSP00000514799.1:n.*905_*906insTCTTTCTCA...
ENST00000308394.9:c.*322_*323insTCTTTCTCAATATT MANE Select ENSP00000311032.4:n.*322_*323insTCTTTCTCA...
ENST00000308394.8:c.*322_*323insTCTTTCTCAATATT ENSP00000311032.4:n.*322_*323insTCTTTCTCA...
ENST00000393585.6:c.*486_*487insTCTTTCTCAATATT ENSP00000377210.2:n.*486_*487insTCTTTCTCA...
ENST00000523916.5:c.*322_*323insTCTTTCTCAATATT ENSP00000428929.1:n.*322_*323insTCTTTCTCA...
ENST00000613118.4:c.*589_*590insTCTTTCTCAATATT ENSP00000478339.1:n.*589_*590insTCTTTCTCA...
NM_004346.3:c.*322_*323insTCTTTCTCAATATT NP_004337.2:n.*322_*323insTCTTTCTCAATATT
NM_032991.2:c.*322_*323insTCTTTCTCAATATT NP_116786.1:n.*322_*323insTCTTTCTCAATATT
XM_011532301.1:c.*322_*323insTCTTTCTCAATATT XP_011530603.1:n.*322_*323insTCTTTCTCAATA...
NM_001354777.1:c.*322_*323insTCTTTCTCAATATT NP_001341706.1:n.*322_*323insTCTTTCTCAATA...
NM_001354779.1:c.*322_*323insTCTTTCTCAATATT NP_001341708.1:n.*322_*323insTCTTTCTCAATA...
NM_001354780.1:c.*322_*323insTCTTTCTCAATATT NP_001341709.1:n.*322_*323insTCTTTCTCAATA...
NM_001354781.1:c.*486_*487insTCTTTCTCAATATT NP_001341710.1:n.*486_*487insTCTTTCTCAATA...
NM_001354782.1:c.*486_*487insTCTTTCTCAATATT NP_001341711.1:n.*486_*487insTCTTTCTCAATA...
NM_001354783.1:c.*486_*487insTCTTTCTCAATATT NP_001341712.1:n.*486_*487insTCTTTCTCAATA...
NM_001354784.1:c.*486_*487insTCTTTCTCAATATT NP_001341713.1:n.*486_*487insTCTTTCTCAATA...
NM_004346.4:c.*322_*323insTCTTTCTCAATATT MANE Select NP_004337.2:n.*322_*323insTCTTTCTCAATATT
NM_001354777.2:c.*322_*323insTCTTTCTCAATATT NP_001341706.1:n.*322_*323insTCTTTCTCAATA...
NM_001354779.2:c.*322_*323insTCTTTCTCAATATT NP_001341708.1:n.*322_*323insTCTTTCTCAATA...
NM_001354780.2:c.*322_*323insTCTTTCTCAATATT NP_001341709.1:n.*322_*323insTCTTTCTCAATA...
NM_001354781.2:c.*486_*487insTCTTTCTCAATATT NP_001341710.1:n.*486_*487insTCTTTCTCAATA...
NM_001354782.2:c.*486_*487insTCTTTCTCAATATT NP_001341711.1:n.*486_*487insTCTTTCTCAATA...
NM_001354783.2:c.*486_*487insTCTTTCTCAATATT NP_001341712.1:n.*486_*487insTCTTTCTCAATA...
NM_001354784.2:c.*486_*487insTCTTTCTCAATATT NP_001341713.1:n.*486_*487insTCTTTCTCAATA...
NM_032991.3:c.*322_*323insTCTTTCTCAATATT NP_116786.1:n.*322_*323insTCTTTCTCAATATT