Canonical Allele Identifier: CA9235709
Gene: CALR HGNC NCBI

Linked Data

ClinVar Variation Id: 2399432
ClinVar RCV Id: RCV004238199
dbSNP Id: rs370869315

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12939511G>A , CM000681.2:g.12939511G>A GRCh38
NC_000019.9:g.13050325G>A , CM000681.1:g.13050325G>A GRCh37
NC_000019.8:g.12911325G>A NCBI36
NG_029662.1:g.5912G>A , LRG_828:g.5912G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000316448.10:c.277G>A MANE Select ENSP00000320866.4:p.Val93Met
ENST00000586760.2:c.277G>A ENSP00000465918.2:p.Val93Met
ENST00000586967.2:c.277G>A ENSP00000466037.2:p.Val93Met
ENST00000588454.6:c.193+276G>A ENSP00000465105.2:n.193+276G>A
ENST00000680816.1:c.277G>A ENSP00000504963.1:p.Val93Met
ENST00000316448.9:c.277G>A ENSP00000320866.4:p.Val93Met
ENST00000587486.6:n.742G>A
ENST00000588454.5:c.193+276G>A ENSP00000465105.1:n.193+276G>A
ENST00000590325.1:n.343G>A
NM_004343.3:c.277G>A , LRG_828t1:c.277G>A NP_004334.1:p.Val93Met
NM_004343.4:c.277G>A MANE Select NP_004334.1:p.Val93Met