Canonical Allele Identifier: CA2683748875

Gene: CALCR

Linked Data

• gnomAD v4: 7-93426334-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426335del , CM000669.2:g.93426335del	GRCh38
NC_000007.13:g.93055647del , CM000669.1:g.93055647del	GRCh37
NC_000007.12:g.92893583del	NCBI36
NG_013005.1:g.153396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*21del MANE Select	ENSP00000389295.1:n.*21del
ENST00000649521.1:c.*21del	ENSP00000497687.1:n.*21del
ENST00000359558.6:c.*21del	ENSP00000352561.2:n.*21del
ENST00000360249.8:c.*956del	ENSP00000353385.5:n.*956del
ENST00000394441.5:c.*21del	ENSP00000377959.1:n.*21del
ENST00000421592.5:c.*21del	ENSP00000399552.1:n.*21del
ENST00000426151.5:c.*21del	ENSP00000389295.1:n.*21del
NM_001164737.1:c.*21del	NP_001158209.1:n.*21del
NM_001164738.1:c.*21del	NP_001158210.1:n.*21del
NM_001742.3:c.*21del	NP_001733.1:n.*21del
NM_001164737.2:c.*21del	NP_001158209.2:n.*21del
NM_001742.4:c.*21del MANE Select	NP_001733.1:n.*21del
NM_001164737.3:c.*21del	NP_001158209.2:n.*21del
NM_001164738.2:c.*21del	NP_001158210.1:n.*21del