Canonical Allele Identifier: CA1114403807
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192537_60192538insC , CM000670.2:g.60192537_60192538insC GRCh38
NC_000008.10:g.61105096_61105097insC , CM000670.1:g.61105096_61105097insC GRCh37
NC_000008.9:g.61267650_61267651insC NCBI36
NG_023193.1:g.93858_93859insG
NG_023193.2:g.93858_93859insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000317995.5:c.*36-2553_*36-2552insG MANE Select ENSP00000314407.4:n.*36-2553_*36-2552insG
ENST00000317995.4:c.*36-2553_*36-2552insG ENSP00000314407.4:n.*36-2553_*36-2552insG
NM_004056.4:c.*36-2553_*36-2552insG NP_004047.3:n.*36-2553_*36-2552insG
XM_011517586.1:c.*36-2553_*36-2552insG XP_011515888.1:n.*36-2553_*36-2552insG
NM_001321839.1:c.*36-2553_*36-2552insG NP_001308768.1:n.*36-2553_*36-2552insG
NM_004056.5:c.*36-2553_*36-2552insG NP_004047.3:n.*36-2553_*36-2552insG
NR_135821.1:n.1235-2553_1235-2552insG
XM_017013818.1:c.*36-2553_*36-2552insG XP_016869307.1:n.*36-2553_*36-2552insG
NM_004056.6:c.*36-2553_*36-2552insG MANE Select NP_004047.3:n.*36-2553_*36-2552insG
NM_001321839.2:c.*36-2553_*36-2552insG NP_001308768.1:n.*36-2553_*36-2552insG
NR_135821.2:n.1212-2553_1212-2552insG