Canonical Allele Identifier: CA9235675
Community Standard Title: NM_004343.4(CALR):c.193+41C>G
Gene: CALR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12939276C>G , CM000681.2:g.12939276C>G GRCh38
NC_000019.9:g.13050090C>G , CM000681.1:g.13050090C>G GRCh37
NC_000019.8:g.12911090C>G NCBI36
NG_029662.1:g.5677C>G , LRG_828:g.5677C>G

Transcript Alleles

HGVS Amino-acid Change
NM_004343.4:c.193+41C>G MANE Select NP_004334.1:n.193+41C>G
ENST00000316448.10:c.193+41C>G MANE Select ENSP00000320866.4:n.193+41C>G
NM_004343.3:c.193+41C>G , LRG_828t1:c.193+41C>G NP_004334.1:n.193+41C>G
ENST00000316448.9:c.193+41C>G ENSP00000320866.4:n.193+41C>G
ENST00000586760.2:c.193+41C>G ENSP00000465918.2:n.193+41C>G
ENST00000586967.2:c.193+41C>G ENSP00000466037.2:n.193+41C>G
ENST00000587486.6:n.658+41C>G
ENST00000588454.5:c.193+41C>G ENSP00000465105.1:n.193+41C>G
ENST00000588454.6:c.193+41C>G ENSP00000465105.2:n.193+41C>G
ENST00000590325.1:n.259+41C>G
ENST00000680816.1:c.193+41C>G ENSP00000504963.1:n.193+41C>G