Canonical Allele Identifier: CA582253936

Gene: CA8

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.60192663_60192665del , CM000670.2:g.60192663_60192665del	GRCh38
NC_000008.10:g.61105222_61105224del , CM000670.1:g.61105222_61105224del	GRCh37
NC_000008.9:g.61267776_61267778del	NCBI36
NG_023193.1:g.93734_93736del
NG_023193.2:g.93734_93736del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317995.5:c.*36-2677_*36-2675del MANE Select	ENSP00000314407.4:n.*36-2677_*36-2675del
ENST00000317995.4:c.*36-2677_*36-2675del	ENSP00000314407.4:n.*36-2677_*36-2675del
NM_004056.4:c.*36-2677_*36-2675del	NP_004047.3:n.*36-2677_*36-2675del
XM_011517586.1:c.*36-2677_*36-2675del	XP_011515888.1:n.*36-2677_*36-2675del
NM_001321839.1:c.*36-2677_*36-2675del	NP_001308768.1:n.*36-2677_*36-2675del
NM_004056.5:c.*36-2677_*36-2675del	NP_004047.3:n.*36-2677_*36-2675del
NR_135821.1:n.1235-2677_1235-2675del
XM_017013818.1:c.*36-2677_*36-2675del	XP_016869307.1:n.*36-2677_*36-2675del
NM_004056.6:c.*36-2677_*36-2675del MANE Select	NP_004047.3:n.*36-2677_*36-2675del
NM_001321839.2:c.*36-2677_*36-2675del	NP_001308768.1:n.*36-2677_*36-2675del
NR_135821.2:n.1212-2677_1212-2675del