Canonical Allele Identifier: CA368214021

Gene: CALCR

Linked Data

• dbSNP Id: rs1200580515
• gnomAD v2: 7-93055684-T-C
• gnomAD v4: 7-93426372-T-C
• COSMIC: COSM2864758 ; COSM2864759
• MyVariant Identifiers: chr7:g.93055684T>C (hg19) ; chr7:g.93426372T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426372T>C , CM000669.2:g.93426372T>C	GRCh38
NC_000007.13:g.93055684T>C , CM000669.1:g.93055684T>C	GRCh37
NC_000007.12:g.92893620T>C	NCBI36
NG_013005.1:g.153359A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1409A>G MANE Select	ENSP00000389295.1:p.Gln470Arg
ENST00000649521.1:c.1457A>G	ENSP00000497687.1:p.Gln486Arg
ENST00000359558.6:c.1511A>G	ENSP00000352561.2:p.Gln504Arg
ENST00000360249.8:c.*919A>G	ENSP00000353385.5:n.*919A>G
ENST00000394441.5:c.1409A>G	ENSP00000377959.1:p.Gln470Arg
ENST00000415529.2:c.1459A>G	ENSP00000413179.1:n.1459A>G
ENST00000421592.5:c.1457A>G	ENSP00000399552.1:p.Gln486Arg
ENST00000423724.5:c.1507A>G	ENSP00000391369.1:n.1507A>G
ENST00000426151.5:c.1409A>G	ENSP00000389295.1:p.Gln470Arg
NM_001164737.1:c.1511A>G	NP_001158209.1:p.Gln504Arg
NM_001164738.1:c.1409A>G	NP_001158210.1:p.Gln470Arg
NM_001742.3:c.1409A>G	NP_001733.1:p.Gln470Arg
NM_001164737.2:c.1457A>G	NP_001158209.2:p.Gln486Arg
NM_001742.4:c.1409A>G MANE Select	NP_001733.1:p.Gln470Arg
NM_001164737.3:c.1457A>G	NP_001158209.2:p.Gln486Arg
NM_001164738.2:c.1409A>G	NP_001158210.1:p.Gln470Arg