Canonical Allele Identifier: CA2683748789

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426205-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426207_93426208dup , CM000669.2:g.93426207_93426208dup	GRCh38
NC_000007.13:g.93055519_93055520dup , CM000669.1:g.93055519_93055520dup	GRCh37
NC_000007.12:g.92893455_92893456dup	NCBI36
NG_013005.1:g.153524_153525dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*149_*150dup MANE Select	ENSP00000389295.1:n.*149_*150dup
ENST00000649521.1:c.*149_*150dup	ENSP00000497687.1:n.*149_*150dup
ENST00000359558.6:c.*149_*150dup	ENSP00000352561.2:n.*149_*150dup
ENST00000421592.5:c.*149_*150dup	ENSP00000399552.1:n.*149_*150dup
NM_001164737.1:c.*149_*150dup	NP_001158209.1:n.*149_*150dup
NM_001164738.1:c.*149_*150dup	NP_001158210.1:n.*149_*150dup
NM_001742.3:c.*149_*150dup	NP_001733.1:n.*149_*150dup
NM_001164737.2:c.*149_*150dup	NP_001158209.2:n.*149_*150dup
NM_001742.4:c.*149_*150dup MANE Select	NP_001733.1:n.*149_*150dup
NM_001164737.3:c.*149_*150dup	NP_001158209.2:n.*149_*150dup
NM_001164738.2:c.*149_*150dup	NP_001158210.1:n.*149_*150dup