Canonical Allele Identifier: CA2683748845

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426287-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426287_93426288insA , CM000669.2:g.93426287_93426288insA	GRCh38
NC_000007.13:g.93055599_93055600insA , CM000669.1:g.93055599_93055600insA	GRCh37
NC_000007.12:g.92893535_92893536insA	NCBI36
NG_013005.1:g.153443_153444insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*68_*69insT MANE Select	ENSP00000389295.1:n.*68_*69insT
ENST00000649521.1:c.*68_*69insT	ENSP00000497687.1:n.*68_*69insT
ENST00000359558.6:c.*68_*69insT	ENSP00000352561.2:n.*68_*69insT
ENST00000421592.5:c.*68_*69insT	ENSP00000399552.1:n.*68_*69insT
NM_001164737.1:c.*68_*69insT	NP_001158209.1:n.*68_*69insT
NM_001164738.1:c.*68_*69insT	NP_001158210.1:n.*68_*69insT
NM_001742.3:c.*68_*69insT	NP_001733.1:n.*68_*69insT
NM_001164737.2:c.*68_*69insT	NP_001158209.2:n.*68_*69insT
NM_001742.4:c.*68_*69insT MANE Select	NP_001733.1:n.*68_*69insT
NM_001164737.3:c.*68_*69insT	NP_001158209.2:n.*68_*69insT
NM_001164738.2:c.*68_*69insT	NP_001158210.1:n.*68_*69insT