Canonical Allele Identifier: CA9235843
Gene: CALR HGNC NCBI

Linked Data

ClinVar Variation Id: 2649360
ClinVar RCV Id: RCV003406862
dbSNP Id: rs149740908

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12940432C>T , CM000681.2:g.12940432C>T GRCh38
NC_000019.9:g.13051246C>T , CM000681.1:g.13051246C>T GRCh37
NC_000019.8:g.12912246C>T NCBI36
NG_029662.1:g.6833C>T , LRG_828:g.6833C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000316448.10:c.682C>T MANE Select ENSP00000320866.4:p.Pro228Ser
ENST00000586760.2:c.682C>T ENSP00000465918.2:p.Pro228Ser
ENST00000586967.2:c.682C>T ENSP00000466037.2:p.Pro228Ser
ENST00000588454.6:c.478C>T ENSP00000465105.2:p.Pro160Ser
ENST00000680816.1:c.682C>T ENSP00000504963.1:p.Pro228Ser
ENST00000316448.9:c.682C>T ENSP00000320866.4:p.Pro228Ser
ENST00000586760.1:c.36C>T
ENST00000588454.5:c.478C>T ENSP00000465105.1:p.Pro160Ser
NM_004343.3:c.682C>T , LRG_828t1:c.682C>T NP_004334.1:p.Pro228Ser
NM_004343.4:c.682C>T MANE Select NP_004334.1:p.Pro228Ser