Canonical Allele Identifier: CA2687785922
Gene: CA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.85328383_85328385del , CM000670.2:g.85328383_85328385del GRCh38
NC_000008.10:g.86240612_86240614del , CM000670.1:g.86240612_86240614del GRCh37
NC_000008.9:g.86427864_86427866del NCBI36
NG_016221.1:g.54735_54737del

Transcript Alleles

HGVS Amino-acid Change
ENST00000523022.6:c.*181_*183del MANE Select ENSP00000429798.1:n.*181_*183del
ENST00000431316.3:c.*181_*183del ENSP00000392338.1:n.*181_*183del
ENST00000523022.5:c.*181_*183del ENSP00000429798.1:n.*181_*183del
ENST00000523953.5:c.*181_*183del ENSP00000430656.1:n.*181_*183del
ENST00000542576.5:c.*181_*183del ENSP00000443517.1:n.*181_*183del
ENST00000626824.1:c.*181_*183del ENSP00000486171.1:n.*181_*183del
NM_001128829.3:c.*181_*183del NP_001122301.1:n.*181_*183del
NM_001128830.3:c.*181_*183del NP_001122302.1:n.*181_*183del
NM_001128831.3:c.*181_*183del NP_001122303.1:n.*181_*183del
NM_001164830.1:c.*181_*183del NP_001158302.1:n.*181_*183del
NM_001291967.1:c.*181_*183del NP_001278896.1:n.*181_*183del
NM_001291968.1:c.*181_*183del NP_001278897.1:n.*181_*183del
NM_001738.4:c.*181_*183del NP_001729.1:n.*181_*183del
XM_011517584.1:c.*181_*183del XP_011515886.1:n.*181_*183del
NM_001128829.4:c.*181_*183del NP_001122301.1:n.*181_*183del
NM_001128830.4:c.*181_*183del NP_001122302.1:n.*181_*183del
NM_001128831.4:c.*181_*183del MANE Select NP_001122303.1:n.*181_*183del
NM_001164830.2:c.*181_*183del NP_001158302.1:n.*181_*183del
NM_001291967.2:c.*181_*183del NP_001278896.1:n.*181_*183del
NM_001291968.2:c.*181_*183del NP_001278897.1:n.*181_*183del
NM_001738.5:c.*181_*183del NP_001729.1:n.*181_*183del