Canonical Allele Identifier: CA576315039

Gene: CALCR

Linked Data

• dbSNP Id: rs1400481140
• gnomAD v2: 7-93055642-A-C
• gnomAD v4: 7-93426330-A-C
• MyVariant Identifiers: chr7:g.93055642A>C (hg19) ; chr7:g.93426330A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426330A>C , CM000669.2:g.93426330A>C	GRCh38
NC_000007.13:g.93055642A>C , CM000669.1:g.93055642A>C	GRCh37
NC_000007.12:g.92893578A>C	NCBI36
NG_013005.1:g.153401T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*26T>G MANE Select	ENSP00000389295.1:n.*26T>G
ENST00000649521.1:c.*26T>G	ENSP00000497687.1:n.*26T>G
ENST00000359558.6:c.*26T>G	ENSP00000352561.2:n.*26T>G
ENST00000360249.8:c.*961T>G	ENSP00000353385.5:n.*961T>G
ENST00000394441.5:c.*26T>G	ENSP00000377959.1:n.*26T>G
ENST00000421592.5:c.*26T>G	ENSP00000399552.1:n.*26T>G
ENST00000426151.5:c.*26T>G	ENSP00000389295.1:n.*26T>G
NM_001164737.1:c.*26T>G	NP_001158209.1:n.*26T>G
NM_001164738.1:c.*26T>G	NP_001158210.1:n.*26T>G
NM_001742.3:c.*26T>G	NP_001733.1:n.*26T>G
NM_001164737.2:c.*26T>G	NP_001158209.2:n.*26T>G
NM_001742.4:c.*26T>G MANE Select	NP_001733.1:n.*26T>G
NM_001164737.3:c.*26T>G	NP_001158209.2:n.*26T>G
NM_001164738.2:c.*26T>G	NP_001158210.1:n.*26T>G