Canonical Allele Identifier: CA2683748856

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426303-T-TCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426303_93426304insCCA , CM000669.2:g.93426303_93426304insCCA	GRCh38
NC_000007.13:g.93055615_93055616insCCA , CM000669.1:g.93055615_93055616insCCA	GRCh37
NC_000007.12:g.92893551_92893552insCCA	NCBI36
NG_013005.1:g.153427_153428insTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*52_*53insTGG MANE Select	ENSP00000389295.1:n.*52_*53insTGG
ENST00000649521.1:c.*52_*53insTGG	ENSP00000497687.1:n.*52_*53insTGG
ENST00000359558.6:c.*52_*53insTGG	ENSP00000352561.2:n.*52_*53insTGG
ENST00000421592.5:c.*52_*53insTGG	ENSP00000399552.1:n.*52_*53insTGG
NM_001164737.1:c.*52_*53insTGG	NP_001158209.1:n.*52_*53insTGG
NM_001164738.1:c.*52_*53insTGG	NP_001158210.1:n.*52_*53insTGG
NM_001742.3:c.*52_*53insTGG	NP_001733.1:n.*52_*53insTGG
NM_001164737.2:c.*52_*53insTGG	NP_001158209.2:n.*52_*53insTGG
NM_001742.4:c.*52_*53insTGG MANE Select	NP_001733.1:n.*52_*53insTGG
NM_001164737.3:c.*52_*53insTGG	NP_001158209.2:n.*52_*53insTGG
NM_001164738.2:c.*52_*53insTGG	NP_001158210.1:n.*52_*53insTGG