Canonical Allele Identifier: CA2683748957
Gene: CALCR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93426693_93426694del , CM000669.2:g.93426693_93426694del GRCh38
NC_000007.13:g.93056005_93056006del , CM000669.1:g.93056005_93056006del GRCh37
NC_000007.12:g.92893941_92893942del NCBI36
NG_013005.1:g.153038_153039del

Transcript Alleles

HGVS Amino-acid Change
ENST00000426151.7:c.1192-104_1192-103del MANE Select ENSP00000389295.1:n.1192-104_1192-103del
ENST00000649521.1:c.1240-104_1240-103del ENSP00000497687.1:n.1240-104_1240-103del
ENST00000359558.6:c.1294-104_1294-103del ENSP00000352561.2:n.1294-104_1294-103del
ENST00000360249.8:c.*702-104_*702-103del ENSP00000353385.5:n.*702-104_*702-103del
ENST00000394441.5:c.1192-104_1192-103del ENSP00000377959.1:n.1192-104_1192-103del
ENST00000415529.2:c.1242-104_1242-103del ENSP00000413179.1:n.1242-104_1242-103del
ENST00000421592.5:c.1240-104_1240-103del ENSP00000399552.1:n.1240-104_1240-103del
ENST00000423724.5:c.1290-104_1290-103del ENSP00000391369.1:n.1290-104_1290-103del
ENST00000426151.5:c.1192-104_1192-103del ENSP00000389295.1:n.1192-104_1192-103del
NM_001164737.1:c.1294-104_1294-103del NP_001158209.1:n.1294-104_1294-103del
NM_001164738.1:c.1192-104_1192-103del NP_001158210.1:n.1192-104_1192-103del
NM_001742.3:c.1192-104_1192-103del NP_001733.1:n.1192-104_1192-103del
NM_001164737.2:c.1240-104_1240-103del NP_001158209.2:n.1240-104_1240-103del
NM_001742.4:c.1192-104_1192-103del MANE Select NP_001733.1:n.1192-104_1192-103del
NM_001164737.3:c.1240-104_1240-103del NP_001158209.2:n.1240-104_1240-103del
NM_001164738.2:c.1192-104_1192-103del NP_001158210.1:n.1192-104_1192-103del