Canonical Allele Identifier: CA582253955
Gene: CA8 HGNC NCBI

Linked Data

dbSNP Id: rs1372083652

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192742_60192745del , CM000670.2:g.60192742_60192745del GRCh38
NC_000008.10:g.61105301_61105304del , CM000670.1:g.61105301_61105304del GRCh37
NC_000008.9:g.61267855_61267858del NCBI36
NG_023193.1:g.93655_93658del
NG_023193.2:g.93655_93658del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317995.5:c.*36-2756_*36-2753del MANE Select ENSP00000314407.4:n.*36-2756_*36-2753del
ENST00000317995.4:c.*36-2756_*36-2753del ENSP00000314407.4:n.*36-2756_*36-2753del
NM_004056.4:c.*36-2756_*36-2753del NP_004047.3:n.*36-2756_*36-2753del
XM_011517586.1:c.*36-2756_*36-2753del XP_011515888.1:n.*36-2756_*36-2753del
NM_001321839.1:c.*36-2756_*36-2753del NP_001308768.1:n.*36-2756_*36-2753del
NM_004056.5:c.*36-2756_*36-2753del NP_004047.3:n.*36-2756_*36-2753del
NR_135821.1:n.1235-2756_1235-2753del
XM_017013818.1:c.*36-2756_*36-2753del XP_016869307.1:n.*36-2756_*36-2753del
NM_004056.6:c.*36-2756_*36-2753del MANE Select NP_004047.3:n.*36-2756_*36-2753del
NM_001321839.2:c.*36-2756_*36-2753del NP_001308768.1:n.*36-2756_*36-2753del
NR_135821.2:n.1212-2756_1212-2753del