Canonical Allele Identifier: CA576707019

Gene: CALCR

Linked Data

• dbSNP Id: rs1562922431
• gnomAD v2: 7-93055800-AGCG-A
• gnomAD v4: 7-93426488-AGCG-A
• MyVariant Identifiers: chr7:g.93055801_93055803del (hg19) ; chr7:g.93426489_93426491del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426491_93426493del , CM000669.2:g.93426491_93426493del	GRCh38
NC_000007.13:g.93055803_93055805del , CM000669.1:g.93055803_93055805del	GRCh37
NC_000007.12:g.92893739_92893741del	NCBI36
NG_013005.1:g.153240_153242del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1290_1292del MANE Select	ENSP00000389295.1:p.Ala431del
ENST00000649521.1:c.1338_1340del	ENSP00000497687.1:p.Ala447del
ENST00000359558.6:c.1392_1394del	ENSP00000352561.2:p.Ala465del
ENST00000360249.8:c.*800_*802del	ENSP00000353385.5:n.*800_*802del
ENST00000394441.5:c.1290_1292del	ENSP00000377959.1:p.Ala431del
ENST00000415529.2:c.1340_1342del	ENSP00000413179.1:n.1340_1342del
ENST00000421592.5:c.1338_1340del	ENSP00000399552.1:p.Ala447del
ENST00000423724.5:c.1388_1390del	ENSP00000391369.1:n.1388_1390del
ENST00000426151.5:c.1290_1292del	ENSP00000389295.1:p.Ala431del
NM_001164737.1:c.1392_1394del	NP_001158209.1:p.Ala465del
NM_001164738.1:c.1290_1292del	NP_001158210.1:p.Ala431del
NM_001742.3:c.1290_1292del	NP_001733.1:p.Ala431del
NM_001164737.2:c.1338_1340del	NP_001158209.2:p.Ala447del
NM_001742.4:c.1290_1292del MANE Select	NP_001733.1:p.Ala431del
NM_001164737.3:c.1338_1340del	NP_001158209.2:p.Ala447del
NM_001164738.2:c.1290_1292del	NP_001158210.1:p.Ala431del