Canonical Allele Identifier: CA2509164565

Gene: CALCR

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426521del , CM000669.2:g.93426521del	GRCh38
NC_000007.13:g.93055833del , CM000669.1:g.93055833del	GRCh37
NC_000007.12:g.92893769del	NCBI36
NG_013005.1:g.153213del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1263del MANE Select	ENSP00000389295.1:p.Ser422ProfsTer26
ENST00000649521.1:c.1311del	ENSP00000497687.1:p.Ser438ProfsTer26
ENST00000359558.6:c.1365del	ENSP00000352561.2:p.Ser456ProfsTer26
ENST00000360249.8:c.*773del	ENSP00000353385.5:n.*773del
ENST00000394441.5:c.1263del	ENSP00000377959.1:p.Ser422ProfsTer26
ENST00000415529.2:c.1313del	ENSP00000413179.1:n.1313del
ENST00000421592.5:c.1311del	ENSP00000399552.1:p.Ser438ProfsTer26
ENST00000423724.5:c.1361del	ENSP00000391369.1:n.1361del
ENST00000426151.5:c.1263del	ENSP00000389295.1:p.Ser422ProfsTer26
NM_001164737.1:c.1365del	NP_001158209.1:p.Ser456ProfsTer26
NM_001164738.1:c.1263del	NP_001158210.1:p.Ser422ProfsTer26
NM_001742.3:c.1263del	NP_001733.1:p.Ser422ProfsTer26
NM_001164737.2:c.1311del	NP_001158209.2:p.Ser438ProfsTer26
NM_001742.4:c.1263del MANE Select	NP_001733.1:p.Ser422ProfsTer26
NM_001164737.3:c.1311del	NP_001158209.2:p.Ser438ProfsTer26
NM_001164738.2:c.1263del	NP_001158210.1:p.Ser422ProfsTer26