Canonical Allele Identifier: CA843977866

Gene: CALCR

Linked Data

• dbSNP Id: rs1329204398
• gnomAD v4: 7-93426073-G-GT
• MyVariant Identifiers: chr7:g.93055385_93055386insT (hg19) ; chr7:g.93426073_93426074insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426078dup , CM000669.2:g.93426078dup	GRCh38
NC_000007.13:g.93055390dup , CM000669.1:g.93055390dup	GRCh37
NC_000007.12:g.92893326dup	NCBI36
NG_013005.1:g.153657dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*282dup MANE Select	ENSP00000389295.1:n.*282dup
ENST00000649521.1:c.*282dup	ENSP00000497687.1:n.*282dup
ENST00000359558.6:c.*282dup	ENSP00000352561.2:n.*282dup
ENST00000421592.5:c.*282dup	ENSP00000399552.1:n.*282dup
NM_001164737.1:c.*282dup	NP_001158209.1:n.*282dup
NM_001164738.1:c.*282dup	NP_001158210.1:n.*282dup
NM_001742.3:c.*282dup	NP_001733.1:n.*282dup
NM_001164737.2:c.*282dup	NP_001158209.2:n.*282dup
NM_001742.4:c.*282dup MANE Select	NP_001733.1:n.*282dup
NM_001164737.3:c.*282dup	NP_001158209.2:n.*282dup
NM_001164738.2:c.*282dup	NP_001158210.1:n.*282dup