Canonical Allele Identifier: CA1787831612
Gene: CA8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192586C= , CM000670.2:g.60192586C= GRCh38
NC_000008.10:g.61105145C= , CM000670.1:g.61105145C= GRCh37
NC_000008.9:g.61267699C= NCBI36
NG_023193.1:g.93810G=
NG_023193.2:g.93810G=

Transcript Alleles

HGVS Amino-acid change
ENST00000317995.5:c.*36-2601G= MANE Select ENSP00000314407.4:n.*36-2601G=
ENST00000317995.4:c.*36-2601G= ENSP00000314407.4:n.*36-2601G=
NM_004056.4:c.*36-2601G= NP_004047.3:n.*36-2601G=
XM_011517586.1:c.*36-2601G= XP_011515888.1:n.*36-2601G=
NM_001321839.1:c.*36-2601G= NP_001308768.1:n.*36-2601G=
NM_004056.5:c.*36-2601G= NP_004047.3:n.*36-2601G=
NR_135821.1:n.1235-2601G=
XM_017013818.1:c.*36-2601G= XP_016869307.1:n.*36-2601G=
NM_004056.6:c.*36-2601G= MANE Select NP_004047.3:n.*36-2601G=
NM_001321839.2:c.*36-2601G= NP_001308768.1:n.*36-2601G=
NR_135821.2:n.1212-2601G=