Canonical Allele Identifier: CA2683748890

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426493-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426494dup , CM000669.2:g.93426494dup	GRCh38
NC_000007.13:g.93055806dup , CM000669.1:g.93055806dup	GRCh37
NC_000007.12:g.92893742dup	NCBI36
NG_013005.1:g.153237dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.1287dup MANE Select	ENSP00000389295.1:p.Ala430SerfsTer21
ENST00000649521.1:c.1335dup	ENSP00000497687.1:p.Ala446SerfsTer21
ENST00000359558.6:c.1389dup	ENSP00000352561.2:p.Ala464SerfsTer21
ENST00000360249.8:c.*797dup	ENSP00000353385.5:n.*797dup
ENST00000394441.5:c.1287dup	ENSP00000377959.1:p.Ala430SerfsTer21
ENST00000415529.2:c.1337dup	ENSP00000413179.1:n.1337dup
ENST00000421592.5:c.1335dup	ENSP00000399552.1:p.Ala446SerfsTer21
ENST00000423724.5:c.1385dup	ENSP00000391369.1:n.1385dup
ENST00000426151.5:c.1287dup	ENSP00000389295.1:p.Ala430SerfsTer21
NM_001164737.1:c.1389dup	NP_001158209.1:p.Ala464SerfsTer21
NM_001164738.1:c.1287dup	NP_001158210.1:p.Ala430SerfsTer21
NM_001742.3:c.1287dup	NP_001733.1:p.Ala430SerfsTer21
NM_001164737.2:c.1335dup	NP_001158209.2:p.Ala446SerfsTer21
NM_001742.4:c.1287dup MANE Select	NP_001733.1:p.Ala430SerfsTer21
NM_001164737.3:c.1335dup	NP_001158209.2:p.Ala446SerfsTer21
NM_001164738.2:c.1287dup	NP_001158210.1:p.Ala430SerfsTer21