Canonical Allele Identifier: CA406472788
Gene: CALM3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46608574C>T , CM000681.2:g.46608574C>T GRCh38
NC_000019.9:g.47111831C>T , CM000681.1:g.47111831C>T GRCh37
NC_000019.8:g.51803671C>T NCBI36
NG_051331.1:g.12501C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000291295.14:c.271C>T MANE Select ENSP00000291295.8:p.Arg91Cys
ENST00000595072.2:n.2700C>T
ENST00000602169.2:c.*307C>T ENSP00000499372.1:n.*307C>T
ENST00000291295.13:c.271C>T ENSP00000291295.8:p.Arg91Cys
ENST00000391918.6:c.163C>T ENSP00000375785.2:p.Arg55Cys
ENST00000477244.5:n.395C>T
ENST00000482455.5:n.381C>T
ENST00000486500.1:n.472C>T
ENST00000594523.5:c.163C>T ENSP00000468877.1:p.Arg55Cys
ENST00000595072.1:n.461C>T
ENST00000596362.1:c.271C>T ENSP00000472141.1:p.Arg91Cys
ENST00000597743.5:c.165+247C>T ENSP00000470308.1:n.165+247C>T
ENST00000597868.5:n.339C>T
ENST00000598871.5:c.163C>T ENSP00000470502.1:p.Arg55Cys
ENST00000599839.5:c.163C>T ENSP00000471225.1:p.Arg55Cys
NM_005184.2:c.271C>T NP_005175.2:p.Arg91Cys
NM_001329921.1:c.163C>T NP_001316850.1:p.Arg55Cys
NM_001329922.1:c.271C>T NP_001316851.1:p.Arg91Cys
NM_001329923.1:c.163C>T NP_001316852.1:p.Arg55Cys
NM_001329924.1:c.163C>T NP_001316853.1:p.Arg55Cys
NM_001329925.1:c.163C>T NP_001316854.1:p.Arg55Cys
NM_001329926.1:c.163C>T NP_001316855.1:p.Arg55Cys
NM_005184.3:c.271C>T NP_005175.2:p.Arg91Cys
NM_001329924.2:c.163C>T NP_001316853.1:p.Arg55Cys
NM_001329925.2:c.163C>T NP_001316854.1:p.Arg55Cys
NM_001329926.2:c.163C>T NP_001316855.1:p.Arg55Cys
NM_005184.4:c.271C>T MANE Select NP_005175.2:p.Arg91Cys