Canonical Allele Identifier: CA162017772

Gene: CALCR

Linked Data

• dbSNP Id: rs983209354
• gnomAD v3: 7-93426144-C-A
• gnomAD v4: 7-93426144-C-A
• MyVariant Identifiers: chr7:g.93055456C>A (hg19) ; chr7:g.93426144C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.93426144C>A , CM000669.2:g.93426144C>A	GRCh38
NC_000007.13:g.93055456C>A , CM000669.1:g.93055456C>A	GRCh37
NC_000007.12:g.92893392C>A	NCBI36
NG_013005.1:g.153587G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000426151.7:c.*212G>T MANE Select	ENSP00000389295.1:n.*212G>T
ENST00000649521.1:c.*212G>T	ENSP00000497687.1:n.*212G>T
ENST00000359558.6:c.*212G>T	ENSP00000352561.2:n.*212G>T
ENST00000421592.5:c.*212G>T	ENSP00000399552.1:n.*212G>T
NM_001164737.1:c.*212G>T	NP_001158209.1:n.*212G>T
NM_001164738.1:c.*212G>T	NP_001158210.1:n.*212G>T
NM_001742.3:c.*212G>T	NP_001733.1:n.*212G>T
NM_001164737.2:c.*212G>T	NP_001158209.2:n.*212G>T
NM_001742.4:c.*212G>T MANE Select	NP_001733.1:n.*212G>T
NM_001164737.3:c.*212G>T	NP_001158209.2:n.*212G>T
NM_001164738.2:c.*212G>T	NP_001158210.1:n.*212G>T