Canonical Allele Identifier: CA2735948942

Gene: CALM3

Linked Data

• dbSNP Id: rs2122247219

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608589_46608590insA , CM000681.2:g.46608589_46608590insA	GRCh38
NC_000019.9:g.47111846_47111847insA , CM000681.1:g.47111846_47111847insA	GRCh37
NC_000019.8:g.51803686_51803687insA	NCBI36
NG_051331.1:g.12516_12517insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291295.14:c.285+1_285+2insA MANE Select	ENSP00000291295.8:n.285+1_285+2insA
ENST00000595072.2:n.2714+1_2714+2insA
ENST00000602169.2:c.*321+1_*321+2insA	ENSP00000499372.1:n.*321+1_*321+2insA
ENST00000291295.13:c.285+1_285+2insA	ENSP00000291295.8:n.285+1_285+2insA
ENST00000391918.6:c.177+1_177+2insA	ENSP00000375785.2:n.177+1_177+2insA
ENST00000477244.5:n.409+1_409+2insA
ENST00000482455.5:n.395+1_395+2insA
ENST00000486500.1:n.487_488insA
ENST00000594523.5:c.177+1_177+2insA	ENSP00000468877.1:n.177+1_177+2insA
ENST00000595072.1:n.475+1_475+2insA
ENST00000596362.1:c.285+1_285+2insA	ENSP00000472141.1:n.285+1_285+2insA
ENST00000597743.5:c.165+262_165+263insA	ENSP00000470308.1:n.165+262_165+263insA
ENST00000597868.5:n.354_355insA
ENST00000598871.5:c.177+1_177+2insA	ENSP00000470502.1:n.177+1_177+2insA
ENST00000599839.5:c.177+1_177+2insA	ENSP00000471225.1:n.177+1_177+2insA
NM_005184.2:c.285+1_285+2insA	NP_005175.2:n.285+1_285+2insA
NM_001329921.1:c.177+1_177+2insA	NP_001316850.1:n.177+1_177+2insA
NM_001329922.1:c.285+1_285+2insA	NP_001316851.1:n.285+1_285+2insA
NM_001329923.1:c.177+1_177+2insA	NP_001316852.1:n.177+1_177+2insA
NM_001329924.1:c.177+1_177+2insA	NP_001316853.1:n.177+1_177+2insA
NM_001329925.1:c.177+1_177+2insA	NP_001316854.1:n.177+1_177+2insA
NM_001329926.1:c.177+1_177+2insA	NP_001316855.1:n.177+1_177+2insA
NM_005184.3:c.285+1_285+2insA	NP_005175.2:n.285+1_285+2insA
NM_001329924.2:c.177+1_177+2insA	NP_001316853.1:n.177+1_177+2insA
NM_001329925.2:c.177+1_177+2insA	NP_001316854.1:n.177+1_177+2insA
NM_001329926.2:c.177+1_177+2insA	NP_001316855.1:n.177+1_177+2insA
NM_005184.4:c.285+1_285+2insA MANE Select	NP_005175.2:n.285+1_285+2insA