Canonical Allele Identifier: CA843977844

Gene: CALCR

Linked Data

• dbSNP Id: rs1289331575
• gnomAD v3: 7-93426043-A-T
• gnomAD v4: 7-93426043-A-T
• MyVariant Identifiers: chr7:g.93055355A>T (hg19) ; chr7:g.93426043A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426043A>T , CM000669.2:g.93426043A>T	GRCh38
NC_000007.13:g.93055355A>T , CM000669.1:g.93055355A>T	GRCh37
NC_000007.12:g.92893291A>T	NCBI36
NG_013005.1:g.153688T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*313T>A MANE Select	ENSP00000389295.1:n.*313T>A
ENST00000649521.1:c.*313T>A	ENSP00000497687.1:n.*313T>A
ENST00000359558.6:c.*313T>A	ENSP00000352561.2:n.*313T>A
ENST00000421592.5:c.*313T>A	ENSP00000399552.1:n.*313T>A
NM_001164737.1:c.*313T>A	NP_001158209.1:n.*313T>A
NM_001164738.1:c.*313T>A	NP_001158210.1:n.*313T>A
NM_001742.3:c.*313T>A	NP_001733.1:n.*313T>A
NM_001164737.2:c.*313T>A	NP_001158209.2:n.*313T>A
NM_001742.4:c.*313T>A MANE Select	NP_001733.1:n.*313T>A
NM_001164737.3:c.*313T>A	NP_001158209.2:n.*313T>A
NM_001164738.2:c.*313T>A	NP_001158210.1:n.*313T>A