Canonical Allele Identifier: CA1726312339

Gene: CALCR

Linked Data

• dbSNP Id: rs1799520780
• gnomAD v4: 7-93426138-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426138A>C , CM000669.2:g.93426138A>C	GRCh38
NC_000007.13:g.93055450A>C , CM000669.1:g.93055450A>C	GRCh37
NC_000007.12:g.92893386A>C	NCBI36
NG_013005.1:g.153593T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*218T>G MANE Select	ENSP00000389295.1:n.*218T>G
ENST00000649521.1:c.*218T>G	ENSP00000497687.1:n.*218T>G
ENST00000359558.6:c.*218T>G	ENSP00000352561.2:n.*218T>G
ENST00000421592.5:c.*218T>G	ENSP00000399552.1:n.*218T>G
NM_001164737.1:c.*218T>G	NP_001158209.1:n.*218T>G
NM_001164738.1:c.*218T>G	NP_001158210.1:n.*218T>G
NM_001742.3:c.*218T>G	NP_001733.1:n.*218T>G
NM_001164737.2:c.*218T>G	NP_001158209.2:n.*218T>G
NM_001742.4:c.*218T>G MANE Select	NP_001733.1:n.*218T>G
NM_001164737.3:c.*218T>G	NP_001158209.2:n.*218T>G
NM_001164738.2:c.*218T>G	NP_001158210.1:n.*218T>G