Canonical Allele Identifier: CA2683748722
Gene: CALCR HGNC NCBI

Linked Data

gnomAD v4: 7-93426084-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93426084A>T , CM000669.2:g.93426084A>T GRCh38
NC_000007.13:g.93055396A>T , CM000669.1:g.93055396A>T GRCh37
NC_000007.12:g.92893332A>T NCBI36
NG_013005.1:g.153647T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000426151.7:c.*272T>A MANE Select ENSP00000389295.1:n.*272T>A
ENST00000649521.1:c.*272T>A ENSP00000497687.1:n.*272T>A
ENST00000359558.6:c.*272T>A ENSP00000352561.2:n.*272T>A
ENST00000421592.5:c.*272T>A ENSP00000399552.1:n.*272T>A
NM_001164737.1:c.*272T>A NP_001158209.1:n.*272T>A
NM_001164738.1:c.*272T>A NP_001158210.1:n.*272T>A
NM_001742.3:c.*272T>A NP_001733.1:n.*272T>A
NM_001164737.2:c.*272T>A NP_001158209.2:n.*272T>A
NM_001742.4:c.*272T>A MANE Select NP_001733.1:n.*272T>A
NM_001164737.3:c.*272T>A NP_001158209.2:n.*272T>A
NM_001164738.2:c.*272T>A NP_001158210.1:n.*272T>A
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