Canonical Allele Identifier: CA2585952688

Gene: CALM3

Linked Data

• gnomAD v4: 19-46608392-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608393_46608394del , CM000681.2:g.46608393_46608394del	GRCh38
NC_000019.9:g.47111650_47111651del , CM000681.1:g.47111650_47111651del	GRCh37
NC_000019.8:g.51803490_51803491del	NCBI36
NG_051331.1:g.12320_12321del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291295.14:c.178+53_178+54del MANE Select	ENSP00000291295.8:n.178+53_178+54del
ENST00000595072.2:n.2607+53_2607+54del
ENST00000602169.2:c.*214+53_*214+54del	ENSP00000499372.1:n.*214+53_*214+54del
ENST00000291295.13:c.178+53_178+54del	ENSP00000291295.8:n.178+53_178+54del
ENST00000391918.6:c.70+53_70+54del	ENSP00000375785.2:n.70+53_70+54del
ENST00000477244.5:n.302+53_302+54del
ENST00000482455.5:n.288+53_288+54del
ENST00000486500.1:n.379+53_379+54del
ENST00000594523.5:c.70+53_70+54del	ENSP00000468877.1:n.70+53_70+54del
ENST00000595072.1:n.368+53_368+54del
ENST00000596362.1:c.178+53_178+54del	ENSP00000472141.1:n.178+53_178+54del
ENST00000597743.5:c.165+66_165+67del	ENSP00000470308.1:n.165+66_165+67del
ENST00000597868.5:n.246+53_246+54del
ENST00000598871.5:c.70+53_70+54del	ENSP00000470502.1:n.70+53_70+54del
ENST00000599839.5:c.70+53_70+54del	ENSP00000471225.1:n.70+53_70+54del
NM_005184.2:c.178+53_178+54del	NP_005175.2:n.178+53_178+54del
NM_001329921.1:c.70+53_70+54del	NP_001316850.1:n.70+53_70+54del
NM_001329922.1:c.178+53_178+54del	NP_001316851.1:n.178+53_178+54del
NM_001329923.1:c.70+53_70+54del	NP_001316852.1:n.70+53_70+54del
NM_001329924.1:c.70+53_70+54del	NP_001316853.1:n.70+53_70+54del
NM_001329925.1:c.70+53_70+54del	NP_001316854.1:n.70+53_70+54del
NM_001329926.1:c.70+53_70+54del	NP_001316855.1:n.70+53_70+54del
NM_005184.3:c.178+53_178+54del	NP_005175.2:n.178+53_178+54del
NM_001329924.2:c.70+53_70+54del	NP_001316853.1:n.70+53_70+54del
NM_001329925.2:c.70+53_70+54del	NP_001316854.1:n.70+53_70+54del
NM_001329926.2:c.70+53_70+54del	NP_001316855.1:n.70+53_70+54del
NM_005184.4:c.178+53_178+54del MANE Select	NP_005175.2:n.178+53_178+54del