Canonical Allele Identifier: CA1726312343
Gene: CALCR HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93426156G= , CM000669.2:g.93426156G= GRCh38
NC_000007.13:g.93055468G= , CM000669.1:g.93055468G= GRCh37
NC_000007.12:g.92893404G= NCBI36
NG_013005.1:g.153575C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000426151.7:c.*200C= MANE Select ENSP00000389295.1:n.*200C=
ENST00000649521.1:c.*200C= ENSP00000497687.1:n.*200C=
ENST00000359558.6:c.*200C= ENSP00000352561.2:n.*200C=
ENST00000421592.5:c.*200C= ENSP00000399552.1:n.*200C=
NM_001164737.1:c.*200C= NP_001158209.1:n.*200C=
NM_001164738.1:c.*200C= NP_001158210.1:n.*200C=
NM_001742.3:c.*200C= NP_001733.1:n.*200C=
NM_001164737.2:c.*200C= NP_001158209.2:n.*200C=
NM_001742.4:c.*200C= MANE Select NP_001733.1:n.*200C=
NM_001164737.3:c.*200C= NP_001158209.2:n.*200C=
NM_001164738.2:c.*200C= NP_001158210.1:n.*200C=
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