Canonical Allele Identifier: CA1787866663
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60237172C= , CM000670.2:g.60237172C= GRCh38
NC_000008.10:g.61149731C= , CM000670.1:g.61149731C= GRCh37
NC_000008.9:g.61312285C= NCBI36
NG_023193.1:g.49224G=
NG_023193.2:g.49224G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000317995.5:c.418-4793G= MANE Select ENSP00000314407.4:n.418-4793G=
ENST00000317995.4:c.418-4793G= ENSP00000314407.4:n.418-4793G=
ENST00000524872.5:n.656-4793G=
NM_004056.4:c.418-4793G= NP_004047.3:n.418-4793G=
XM_011517585.1:c.418-4793G= XP_011515887.1:n.418-4793G=
XM_011517586.1:c.418-10237G= XP_011515888.1:n.418-10237G=
NM_001321837.1:c.418-4793G= NP_001308766.1:n.418-4793G=
NM_001321838.1:c.418-4793G= NP_001308767.1:n.418-4793G=
NM_001321839.1:c.418-10237G= NP_001308768.1:n.418-10237G=
NM_004056.5:c.418-4793G= NP_004047.3:n.418-4793G=
NR_135821.1:n.694-4793G=
XM_017013818.1:c.166-4793G= XP_016869307.1:n.166-4793G=
NM_004056.6:c.418-4793G= MANE Select NP_004047.3:n.418-4793G=
NM_001321837.2:c.418-4793G= NP_001308766.1:n.418-4793G=
NM_001321838.2:c.418-4793G= NP_001308767.1:n.418-4793G=
NM_001321839.2:c.418-10237G= NP_001308768.1:n.418-10237G=
NR_135821.2:n.671-4793G=