Canonical Allele Identifier: CA576315020

Gene: CALCR

Linked Data

• dbSNP Id: rs1365066727
• gnomAD v2: 7-93055375-C-CT
• gnomAD v3: 7-93426063-C-CT
• gnomAD v4: 7-93426063-C-CT
• MyVariant Identifiers: chr7:g.93055375_93055376insT (hg19) ; chr7:g.93426063_93426064insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426063_93426064insT , CM000669.2:g.93426063_93426064insT	GRCh38
NC_000007.13:g.93055375_93055376insT , CM000669.1:g.93055375_93055376insT	GRCh37
NC_000007.12:g.92893311_92893312insT	NCBI36
NG_013005.1:g.153667_153668insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*292_*293insA MANE Select	ENSP00000389295.1:n.*292_*293insA
ENST00000649521.1:c.*292_*293insA	ENSP00000497687.1:n.*292_*293insA
ENST00000359558.6:c.*292_*293insA	ENSP00000352561.2:n.*292_*293insA
ENST00000421592.5:c.*292_*293insA	ENSP00000399552.1:n.*292_*293insA
NM_001164737.1:c.*292_*293insA	NP_001158209.1:n.*292_*293insA
NM_001164738.1:c.*292_*293insA	NP_001158210.1:n.*292_*293insA
NM_001742.3:c.*292_*293insA	NP_001733.1:n.*292_*293insA
NM_001164737.2:c.*292_*293insA	NP_001158209.2:n.*292_*293insA
NM_001742.4:c.*292_*293insA MANE Select	NP_001733.1:n.*292_*293insA
NM_001164737.3:c.*292_*293insA	NP_001158209.2:n.*292_*293insA
NM_001164738.2:c.*292_*293insA	NP_001158210.1:n.*292_*293insA