Canonical Allele Identifier: CA1104526797
Gene: CALCR HGNC NCBI

Linked Data

dbSNP Id: rs1799521861
gnomAD v3: 7-93426205-CTT-C
gnomAD v4: 7-93426205-CTT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93426207_93426208del , CM000669.2:g.93426207_93426208del GRCh38
NC_000007.13:g.93055519_93055520del , CM000669.1:g.93055519_93055520del GRCh37
NC_000007.12:g.92893455_92893456del NCBI36
NG_013005.1:g.153524_153525del

Transcript Alleles

HGVS Amino-acid Change
ENST00000426151.7:c.*149_*150del MANE Select ENSP00000389295.1:n.*149_*150del
ENST00000649521.1:c.*149_*150del ENSP00000497687.1:n.*149_*150del
ENST00000359558.6:c.*149_*150del ENSP00000352561.2:n.*149_*150del
ENST00000421592.5:c.*149_*150del ENSP00000399552.1:n.*149_*150del
NM_001164737.1:c.*149_*150del NP_001158209.1:n.*149_*150del
NM_001164738.1:c.*149_*150del NP_001158210.1:n.*149_*150del
NM_001742.3:c.*149_*150del NP_001733.1:n.*149_*150del
NM_001164737.2:c.*149_*150del NP_001158209.2:n.*149_*150del
NM_001742.4:c.*149_*150del MANE Select NP_001733.1:n.*149_*150del
NM_001164737.3:c.*149_*150del NP_001158209.2:n.*149_*150del
NM_001164738.2:c.*149_*150del NP_001158210.1:n.*149_*150del
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