Canonical Allele Identifier: CA1787831767
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192686_60192689delinsATAT , CM000670.2:g.60192686_60192689delinsATAT GRCh38
NC_000008.10:g.61105245_61105248delinsATAT , CM000670.1:g.61105245_61105248delinsATAT GRCh37
NC_000008.9:g.61267799_61267802delinsATAT NCBI36
NG_023193.1:g.93707_93710delinsATAT
NG_023193.2:g.93707_93710delinsATAT

Transcript Alleles

HGVS Amino-acid change
ENST00000317995.5:c.*36-2704_*36-2701delinsATAT MANE Select ENSP00000314407.4:n.*36-2704_*36-2701delinsATAT
ENST00000317995.4:c.*36-2704_*36-2701delinsATAT ENSP00000314407.4:n.*36-2704_*36-2701delinsATAT
NM_004056.4:c.*36-2704_*36-2701delinsATAT NP_004047.3:n.*36-2704_*36-2701delinsATAT
XM_011517586.1:c.*36-2704_*36-2701delinsATAT XP_011515888.1:n.*36-2704_*36-2701delinsATAT
NM_001321839.1:c.*36-2704_*36-2701delinsATAT NP_001308768.1:n.*36-2704_*36-2701delinsATAT
NM_004056.5:c.*36-2704_*36-2701delinsATAT NP_004047.3:n.*36-2704_*36-2701delinsATAT
NR_135821.1:n.1235-2704_1235-2701delinsATAT
XM_017013818.1:c.*36-2704_*36-2701delinsATAT XP_016869307.1:n.*36-2704_*36-2701delinsATAT
NM_004056.6:c.*36-2704_*36-2701delinsATAT MANE Select NP_004047.3:n.*36-2704_*36-2701delinsATAT
NM_001321839.2:c.*36-2704_*36-2701delinsATAT NP_001308768.1:n.*36-2704_*36-2701delinsATAT
NR_135821.2:n.1212-2704_1212-2701delinsATAT