Canonical Allele Identifier: CA2683748785
Gene: CALCR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93426202_93426203insGTA , CM000669.2:g.93426202_93426203insGTA GRCh38
NC_000007.13:g.93055514_93055515insGTA , CM000669.1:g.93055514_93055515insGTA GRCh37
NC_000007.12:g.92893450_92893451insGTA NCBI36
NG_013005.1:g.153528_153529insTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000426151.7:c.*153_*154insTAC MANE Select ENSP00000389295.1:n.*153_*154insTAC
ENST00000649521.1:c.*153_*154insTAC ENSP00000497687.1:n.*153_*154insTAC
ENST00000359558.6:c.*153_*154insTAC ENSP00000352561.2:n.*153_*154insTAC
ENST00000421592.5:c.*153_*154insTAC ENSP00000399552.1:n.*153_*154insTAC
NM_001164737.1:c.*153_*154insTAC NP_001158209.1:n.*153_*154insTAC
NM_001164738.1:c.*153_*154insTAC NP_001158210.1:n.*153_*154insTAC
NM_001742.3:c.*153_*154insTAC NP_001733.1:n.*153_*154insTAC
NM_001164737.2:c.*153_*154insTAC NP_001158209.2:n.*153_*154insTAC
NM_001742.4:c.*153_*154insTAC MANE Select NP_001733.1:n.*153_*154insTAC
NM_001164737.3:c.*153_*154insTAC NP_001158209.2:n.*153_*154insTAC
NM_001164738.2:c.*153_*154insTAC NP_001158210.1:n.*153_*154insTAC