Canonical Allele Identifier: CA14635946
Community Standard Title: NM_004343.4(CALR):c.961-239G>A
Gene: CALR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.12943298G>A , CM000681.2:g.12943298G>A GRCh38
NC_000019.9:g.13054112G>A , CM000681.1:g.13054112G>A GRCh37
NC_000019.8:g.12915112G>A NCBI36
NG_029662.1:g.9699G>A , LRG_828:g.9699G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004343.4:c.961-239G>A MANE Select NP_004334.1:n.961-239G>A
ENST00000316448.10:c.961-239G>A MANE Select ENSP00000320866.4:n.961-239G>A
NM_004343.3:c.961-239G>A , LRG_828t1:c.961-239G>A NP_004334.1:n.961-239G>A
ENST00000316448.9:c.961-239G>A ENSP00000320866.4:n.961-239G>A
ENST00000586760.1:c.315-239G>A
ENST00000586760.2:c.961-239G>A ENSP00000465918.2:n.961-239G>A
ENST00000586803.1:n.86G>A
ENST00000586967.2:c.961-239G>A ENSP00000466037.2:n.961-239G>A
ENST00000588454.6:c.757-239G>A ENSP00000465105.2:n.757-239G>A
ENST00000680816.1:c.1049-239G>A ENSP00000504963.1:n.1049-239G>A