Canonical Allele Identifier: CA406472296
Gene: CALM3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46608340G>C , CM000681.2:g.46608340G>C GRCh38
NC_000019.9:g.47111597G>C , CM000681.1:g.47111597G>C GRCh37
NC_000019.8:g.51803437G>C NCBI36
NG_051331.1:g.12267G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000291295.14:c.178G>C MANE Select ENSP00000291295.8:p.Gly60Arg
ENST00000595072.2:n.2607G>C
ENST00000602169.2:c.*214G>C ENSP00000499372.1:n.*214G>C
ENST00000291295.13:c.178G>C ENSP00000291295.8:p.Gly60Arg
ENST00000391918.6:c.70G>C ENSP00000375785.2:p.Gly24Arg
ENST00000477244.5:n.302G>C
ENST00000482455.5:n.288G>C
ENST00000486500.1:n.379G>C
ENST00000594523.5:c.70G>C ENSP00000468877.1:p.Gly24Arg
ENST00000595072.1:n.368G>C
ENST00000596362.1:c.178G>C ENSP00000472141.1:p.Gly60Arg
ENST00000597743.5:c.165+13G>C ENSP00000470308.1:n.165+13G>C
ENST00000597868.5:n.246G>C
ENST00000598871.5:c.70G>C ENSP00000470502.1:p.Gly24Arg
ENST00000599839.5:c.70G>C ENSP00000471225.1:p.Gly24Arg
NM_005184.2:c.178G>C NP_005175.2:p.Gly60Arg
NM_001329921.1:c.70G>C NP_001316850.1:p.Gly24Arg
NM_001329922.1:c.178G>C NP_001316851.1:p.Gly60Arg
NM_001329923.1:c.70G>C NP_001316852.1:p.Gly24Arg
NM_001329924.1:c.70G>C NP_001316853.1:p.Gly24Arg
NM_001329925.1:c.70G>C NP_001316854.1:p.Gly24Arg
NM_001329926.1:c.70G>C NP_001316855.1:p.Gly24Arg
NM_005184.3:c.178G>C NP_005175.2:p.Gly60Arg
NM_001329924.2:c.70G>C NP_001316853.1:p.Gly24Arg
NM_001329925.2:c.70G>C NP_001316854.1:p.Gly24Arg
NM_001329926.2:c.70G>C NP_001316855.1:p.Gly24Arg
NM_005184.4:c.178G>C MANE Select NP_005175.2:p.Gly60Arg