Canonical Allele Identifier: CA15947527
Gene: CALR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12941177A>G , CM000681.2:g.12941177A>G GRCh38
NC_000019.9:g.13051991A>G , CM000681.1:g.13051991A>G GRCh37
NC_000019.8:g.12912991A>G NCBI36
NG_029662.1:g.7578A>G , LRG_828:g.7578A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000316448.10:c.960+290A>G MANE Select ENSP00000320866.4:n.960+290A>G
ENST00000586760.2:c.960+290A>G ENSP00000465918.2:n.960+290A>G
ENST00000586967.2:c.960+290A>G ENSP00000466037.2:n.960+290A>G
ENST00000588454.6:c.756+290A>G ENSP00000465105.2:n.756+290A>G
ENST00000680816.1:c.1048+202A>G ENSP00000504963.1:n.1048+202A>G
ENST00000316448.9:c.960+290A>G ENSP00000320866.4:n.960+290A>G
ENST00000586760.1:c.314+290A>G
NM_004343.3:c.960+290A>G , LRG_828t1:c.960+290A>G NP_004334.1:n.960+290A>G
NM_004343.4:c.960+290A>G MANE Select NP_004334.1:n.960+290A>G