Canonical Allele Identifier: CA1787831519
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192516_60192517delinsTG , CM000670.2:g.60192516_60192517delinsTG GRCh38
NC_000008.10:g.61105075_61105076delinsTG , CM000670.1:g.61105075_61105076delinsTG GRCh37
NC_000008.9:g.61267629_61267630delinsTG NCBI36
NG_023193.1:g.93879_93880delinsCA
NG_023193.2:g.93879_93880delinsCA

Transcript Alleles

HGVS Amino-acid change
ENST00000317995.5:c.*36-2532_*36-2531delinsCA MANE Select ENSP00000314407.4:n.*36-2532_*36-2531deli...
ENST00000317995.4:c.*36-2532_*36-2531delinsCA ENSP00000314407.4:n.*36-2532_*36-2531deli...
NM_004056.4:c.*36-2532_*36-2531delinsCA NP_004047.3:n.*36-2532_*36-2531delinsCA
XM_011517586.1:c.*36-2532_*36-2531delinsCA XP_011515888.1:n.*36-2532_*36-2531delinsC...
NM_001321839.1:c.*36-2532_*36-2531delinsCA NP_001308768.1:n.*36-2532_*36-2531delinsC...
NM_004056.5:c.*36-2532_*36-2531delinsCA NP_004047.3:n.*36-2532_*36-2531delinsCA
NR_135821.1:n.1235-2532_1235-2531delinsCA
XM_017013818.1:c.*36-2532_*36-2531delinsCA XP_016869307.1:n.*36-2532_*36-2531delinsC...
NM_004056.6:c.*36-2532_*36-2531delinsCA MANE Select NP_004047.3:n.*36-2532_*36-2531delinsCA
NM_001321839.2:c.*36-2532_*36-2531delinsCA NP_001308768.1:n.*36-2532_*36-2531delinsC...
NR_135821.2:n.1212-2532_1212-2531delinsCA