Canonical Allele Identifier: CA2585952925

Gene: CALM3

Linked Data

• gnomAD v4: 19-46608848-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608851del , CM000681.2:g.46608851del	GRCh38
NC_000019.9:g.47112108del , CM000681.1:g.47112108del	GRCh37
NC_000019.8:g.51803948del	NCBI36
NG_051331.1:g.12778del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291295.14:c.291del MANE Select	ENSP00000291295.8:p.Asn98MetfsTer12
ENST00000595072.2:n.2720del
ENST00000602169.2:c.*327del	ENSP00000499372.1:n.*327del
ENST00000291295.13:c.291del	ENSP00000291295.8:p.Asn98MetfsTer12
ENST00000391918.6:c.183del	ENSP00000375785.2:p.Asn62MetfsTer12
ENST00000477244.5:n.415del
ENST00000482455.5:n.401del
ENST00000486500.1:n.749del
ENST00000594523.5:c.183del	ENSP00000468877.1:p.Asn62MetfsTer12
ENST00000595072.1:n.481del
ENST00000596362.1:c.291del	ENSP00000472141.1:p.Asn98MetfsTer12
ENST00000597743.5:c.166-73del	ENSP00000470308.1:n.166-73del
ENST00000597868.5:n.616del
ENST00000598871.5:c.183del	ENSP00000470502.1:p.Asn62MetfsTer12
ENST00000599839.5:c.183del	ENSP00000471225.1:p.Asn62MetfsTer12
NM_005184.2:c.291del	NP_005175.2:p.Asn98MetfsTer12
NM_001329921.1:c.183del	NP_001316850.1:p.Asn62MetfsTer12
NM_001329922.1:c.291del	NP_001316851.1:p.Asn98MetfsTer12
NM_001329923.1:c.183del	NP_001316852.1:p.Asn62MetfsTer12
NM_001329924.1:c.183del	NP_001316853.1:p.Asn62MetfsTer12
NM_001329925.1:c.183del	NP_001316854.1:p.Asn62MetfsTer12
NM_001329926.1:c.183del	NP_001316855.1:p.Asn62MetfsTer12
NM_005184.3:c.291del	NP_005175.2:p.Asn98MetfsTer12
NM_001329924.2:c.183del	NP_001316853.1:p.Asn62MetfsTer12
NM_001329925.2:c.183del	NP_001316854.1:p.Asn62MetfsTer12
NM_001329926.2:c.183del	NP_001316855.1:p.Asn62MetfsTer12
NM_005184.4:c.291del MANE Select	NP_005175.2:p.Asn98MetfsTer12