Canonical Allele Identifier: CA1787831481
Gene: CA8 HGNC NCBI

Linked Data

dbSNP Id: rs1806158344
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192498dup , CM000670.2:g.60192498dup GRCh38
NC_000008.10:g.61105057dup , CM000670.1:g.61105057dup GRCh37
NC_000008.9:g.61267611dup NCBI36
NG_023193.1:g.93899dup
NG_023193.2:g.93899dup

Transcript Alleles

HGVS Amino-acid change
ENST00000317995.5:c.*36-2512dup MANE Select ENSP00000314407.4:n.*36-2512dup
ENST00000317995.4:c.*36-2512dup ENSP00000314407.4:n.*36-2512dup
NM_004056.4:c.*36-2512dup NP_004047.3:n.*36-2512dup
XM_011517586.1:c.*36-2512dup XP_011515888.1:n.*36-2512dup
NM_001321839.1:c.*36-2512dup NP_001308768.1:n.*36-2512dup
NM_004056.5:c.*36-2512dup NP_004047.3:n.*36-2512dup
NR_135821.1:n.1235-2512dup
XM_017013818.1:c.*36-2512dup XP_016869307.1:n.*36-2512dup
NM_004056.6:c.*36-2512dup MANE Select NP_004047.3:n.*36-2512dup
NM_001321839.2:c.*36-2512dup NP_001308768.1:n.*36-2512dup
NR_135821.2:n.1212-2512dup
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