Canonical Allele Identifier: CA1726312547
Gene: CALCR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.93426588_93426593delinsACCTGG , CM000669.2:g.93426588_93426593delinsACCTGG GRCh38
NC_000007.13:g.93055900_93055905delinsACCTGG , CM000669.1:g.93055900_93055905delinsACCTGG GRCh37
NC_000007.12:g.92893836_92893841delinsACCTGG NCBI36
NG_013005.1:g.153138_153143delinsCCAGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000426151.7:c.1192-4_1193delinsCCAGGT
ENST00000649521.1:c.1240-4_1241delinsCCAGGT
ENST00000359558.6:c.1294-4_1295delinsCCAGGT
ENST00000360249.8:c.*702-4_*703delinsCCAGGT
ENST00000394441.5:c.1192-4_1193delinsCCAGGT
ENST00000415529.2:c.1242-4_1243delinsCCAGGT
ENST00000421592.5:c.1240-4_1241delinsCCAGGT
ENST00000423724.5:c.1290-4_1291delinsCCAGGT
ENST00000426151.5:c.1192-4_1193delinsCCAGGT
NM_001164737.1:c.1294-4_1295delinsCCAGGT
NM_001164738.1:c.1192-4_1193delinsCCAGGT
NM_001742.3:c.1192-4_1193delinsCCAGGT
NM_001164737.2:c.1240-4_1241delinsCCAGGT
NM_001742.4:c.1192-4_1193delinsCCAGGT
NM_001164737.3:c.1240-4_1241delinsCCAGGT
NM_001164738.2:c.1192-4_1193delinsCCAGGT