Canonical Allele Identifier: CA2338996056
Gene: CALM3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.46608371_46608374delinsGCTC , CM000681.2:g.46608371_46608374delinsGCTC GRCh38
NC_000019.9:g.47111628_47111631delinsGCTC , CM000681.1:g.47111628_47111631delinsGCTC GRCh37
NC_000019.8:g.51803468_51803471delinsGCTC NCBI36
NG_051331.1:g.12298_12301delinsGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000291295.14:c.178+31_178+34delinsGCTC MANE Select ENSP00000291295.8:n.178+31_178+34delinsGCTC
ENST00000595072.2:n.2607+31_2607+34delinsGCTC
ENST00000602169.2:c.*214+31_*214+34delinsGCTC ENSP00000499372.1:n.*214+31_*214+34delinsGCTC
ENST00000291295.13:c.178+31_178+34delinsGCTC ENSP00000291295.8:n.178+31_178+34delinsGCTC
ENST00000391918.6:c.70+31_70+34delinsGCTC ENSP00000375785.2:n.70+31_70+34delinsGCTC
ENST00000477244.5:n.302+31_302+34delinsGCTC
ENST00000482455.5:n.288+31_288+34delinsGCTC
ENST00000486500.1:n.379+31_379+34delinsGCTC
ENST00000594523.5:c.70+31_70+34delinsGCTC ENSP00000468877.1:n.70+31_70+34delinsGCTC
ENST00000595072.1:n.368+31_368+34delinsGCTC
ENST00000596362.1:c.178+31_178+34delinsGCTC ENSP00000472141.1:n.178+31_178+34delinsGCTC
ENST00000597743.5:c.165+44_165+47delinsGCTC ENSP00000470308.1:n.165+44_165+47delinsGCTC
ENST00000597868.5:n.246+31_246+34delinsGCTC
ENST00000598871.5:c.70+31_70+34delinsGCTC ENSP00000470502.1:n.70+31_70+34delinsGCTC
ENST00000599839.5:c.70+31_70+34delinsGCTC ENSP00000471225.1:n.70+31_70+34delinsGCTC
NM_005184.2:c.178+31_178+34delinsGCTC NP_005175.2:n.178+31_178+34delinsGCTC
NM_001329921.1:c.70+31_70+34delinsGCTC NP_001316850.1:n.70+31_70+34delinsGCTC
NM_001329922.1:c.178+31_178+34delinsGCTC NP_001316851.1:n.178+31_178+34delinsGCTC
NM_001329923.1:c.70+31_70+34delinsGCTC NP_001316852.1:n.70+31_70+34delinsGCTC
NM_001329924.1:c.70+31_70+34delinsGCTC NP_001316853.1:n.70+31_70+34delinsGCTC
NM_001329925.1:c.70+31_70+34delinsGCTC NP_001316854.1:n.70+31_70+34delinsGCTC
NM_001329926.1:c.70+31_70+34delinsGCTC NP_001316855.1:n.70+31_70+34delinsGCTC
NM_005184.3:c.178+31_178+34delinsGCTC NP_005175.2:n.178+31_178+34delinsGCTC
NM_001329924.2:c.70+31_70+34delinsGCTC NP_001316853.1:n.70+31_70+34delinsGCTC
NM_001329925.2:c.70+31_70+34delinsGCTC NP_001316854.1:n.70+31_70+34delinsGCTC
NM_001329926.2:c.70+31_70+34delinsGCTC NP_001316855.1:n.70+31_70+34delinsGCTC
NM_005184.4:c.178+31_178+34delinsGCTC MANE Select NP_005175.2:n.178+31_178+34delinsGCTC