Canonical Allele Identifier: CA853842318
Gene: CA8 HGNC NCBI

Linked Data

dbSNP Id: rs1469765776
MyVariant Identifiers: chr8:g.61105008_61105011del (hg19) chr8:g.60192449_60192452del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.60192451_60192454del , CM000670.2:g.60192451_60192454del GRCh38
NC_000008.10:g.61105010_61105013del , CM000670.1:g.61105010_61105013del GRCh37
NC_000008.9:g.61267564_61267567del NCBI36
NG_023193.1:g.93944_93947del
NG_023193.2:g.93944_93947del

Transcript Alleles

HGVS Amino-acid change
ENST00000317995.5:c.*36-2467_*36-2464del MANE Select ENSP00000314407.4:n.*36-2467_*36-2464del
ENST00000317995.4:c.*36-2467_*36-2464del ENSP00000314407.4:n.*36-2467_*36-2464del
NM_004056.4:c.*36-2467_*36-2464del NP_004047.3:n.*36-2467_*36-2464del
XM_011517586.1:c.*36-2467_*36-2464del XP_011515888.1:n.*36-2467_*36-2464del
NM_001321839.1:c.*36-2467_*36-2464del NP_001308768.1:n.*36-2467_*36-2464del
NM_004056.5:c.*36-2467_*36-2464del NP_004047.3:n.*36-2467_*36-2464del
NR_135821.1:n.1235-2467_1235-2464del
XM_017013818.1:c.*36-2467_*36-2464del XP_016869307.1:n.*36-2467_*36-2464del
NM_004056.6:c.*36-2467_*36-2464del MANE Select NP_004047.3:n.*36-2467_*36-2464del
NM_001321839.2:c.*36-2467_*36-2464del NP_001308768.1:n.*36-2467_*36-2464del
NR_135821.2:n.1212-2467_1212-2464del
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