Canonical Allele Identifier: CA1787831651
Gene: CA8 HGNC NCBI

Linked Data

dbSNP Id: rs1806161878

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192628A>T , CM000670.2:g.60192628A>T GRCh38
NC_000008.10:g.61105187A>T , CM000670.1:g.61105187A>T GRCh37
NC_000008.9:g.61267741A>T NCBI36
NG_023193.1:g.93768T>A
NG_023193.2:g.93768T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000317995.5:c.*36-2643T>A MANE Select ENSP00000314407.4:n.*36-2643T>A
ENST00000317995.4:c.*36-2643T>A ENSP00000314407.4:n.*36-2643T>A
NM_004056.4:c.*36-2643T>A NP_004047.3:n.*36-2643T>A
XM_011517586.1:c.*36-2643T>A XP_011515888.1:n.*36-2643T>A
NM_001321839.1:c.*36-2643T>A NP_001308768.1:n.*36-2643T>A
NM_004056.5:c.*36-2643T>A NP_004047.3:n.*36-2643T>A
NR_135821.1:n.1235-2643T>A
XM_017013818.1:c.*36-2643T>A XP_016869307.1:n.*36-2643T>A
NM_004056.6:c.*36-2643T>A MANE Select NP_004047.3:n.*36-2643T>A
NM_001321839.2:c.*36-2643T>A NP_001308768.1:n.*36-2643T>A
NR_135821.2:n.1212-2643T>A