Canonical Allele Identifier: CA2585952671

Gene: CALM3

Linked Data

• gnomAD v4: 19-46608353-G-GTGT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608353_46608354insTGT , CM000681.2:g.46608353_46608354insTGT	GRCh38
NC_000019.9:g.47111610_47111611insTGT , CM000681.1:g.47111610_47111611insTGT	GRCh37
NC_000019.8:g.51803450_51803451insTGT	NCBI36
NG_051331.1:g.12280_12281insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291295.14:c.178+13_178+14insTGT MANE Select	ENSP00000291295.8:n.178+13_178+14insTGT
ENST00000595072.2:n.2607+13_2607+14insTGT
ENST00000602169.2:c.*214+13_*214+14insTGT	ENSP00000499372.1:n.*214+13_*214+14insTGT
ENST00000291295.13:c.178+13_178+14insTGT	ENSP00000291295.8:n.178+13_178+14insTGT
ENST00000391918.6:c.70+13_70+14insTGT	ENSP00000375785.2:n.70+13_70+14insTGT
ENST00000477244.5:n.302+13_302+14insTGT
ENST00000482455.5:n.288+13_288+14insTGT
ENST00000486500.1:n.379+13_379+14insTGT
ENST00000594523.5:c.70+13_70+14insTGT	ENSP00000468877.1:n.70+13_70+14insTGT
ENST00000595072.1:n.368+13_368+14insTGT
ENST00000596362.1:c.178+13_178+14insTGT	ENSP00000472141.1:n.178+13_178+14insTGT
ENST00000597743.5:c.165+26_165+27insTGT	ENSP00000470308.1:n.165+26_165+27insTGT
ENST00000597868.5:n.246+13_246+14insTGT
ENST00000598871.5:c.70+13_70+14insTGT	ENSP00000470502.1:n.70+13_70+14insTGT
ENST00000599839.5:c.70+13_70+14insTGT	ENSP00000471225.1:n.70+13_70+14insTGT
NM_005184.2:c.178+13_178+14insTGT	NP_005175.2:n.178+13_178+14insTGT
NM_001329921.1:c.70+13_70+14insTGT	NP_001316850.1:n.70+13_70+14insTGT
NM_001329922.1:c.178+13_178+14insTGT	NP_001316851.1:n.178+13_178+14insTGT
NM_001329923.1:c.70+13_70+14insTGT	NP_001316852.1:n.70+13_70+14insTGT
NM_001329924.1:c.70+13_70+14insTGT	NP_001316853.1:n.70+13_70+14insTGT
NM_001329925.1:c.70+13_70+14insTGT	NP_001316854.1:n.70+13_70+14insTGT
NM_001329926.1:c.70+13_70+14insTGT	NP_001316855.1:n.70+13_70+14insTGT
NM_005184.3:c.178+13_178+14insTGT	NP_005175.2:n.178+13_178+14insTGT
NM_001329924.2:c.70+13_70+14insTGT	NP_001316853.1:n.70+13_70+14insTGT
NM_001329925.2:c.70+13_70+14insTGT	NP_001316854.1:n.70+13_70+14insTGT
NM_001329926.2:c.70+13_70+14insTGT	NP_001316855.1:n.70+13_70+14insTGT
NM_005184.4:c.178+13_178+14insTGT MANE Select	NP_005175.2:n.178+13_178+14insTGT