Canonical Allele Identifier: CA853842406
Gene: CA8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192642_60192643del , CM000670.2:g.60192642_60192643del GRCh38
NC_000008.10:g.61105201_61105202del , CM000670.1:g.61105201_61105202del GRCh37
NC_000008.9:g.61267755_61267756del NCBI36
NG_023193.1:g.93761_93762del
NG_023193.2:g.93761_93762del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317995.5:c.*36-2650_*36-2649del MANE Select ENSP00000314407.4:n.*36-2650_*36-2649del
ENST00000317995.4:c.*36-2650_*36-2649del ENSP00000314407.4:n.*36-2650_*36-2649del
NM_004056.4:c.*36-2650_*36-2649del NP_004047.3:n.*36-2650_*36-2649del
XM_011517586.1:c.*36-2650_*36-2649del XP_011515888.1:n.*36-2650_*36-2649del
NM_001321839.1:c.*36-2650_*36-2649del NP_001308768.1:n.*36-2650_*36-2649del
NM_004056.5:c.*36-2650_*36-2649del NP_004047.3:n.*36-2650_*36-2649del
NR_135821.1:n.1235-2650_1235-2649del
XM_017013818.1:c.*36-2650_*36-2649del XP_016869307.1:n.*36-2650_*36-2649del
NM_004056.6:c.*36-2650_*36-2649del MANE Select NP_004047.3:n.*36-2650_*36-2649del
NM_001321839.2:c.*36-2650_*36-2649del NP_001308768.1:n.*36-2650_*36-2649del
NR_135821.2:n.1212-2650_1212-2649del
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