Canonical Allele Identifier: CA2338996204

Gene: CALM3

Linked Data

• dbSNP Id: rs1971800245
• gnomAD v4: 19-46608770-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608770T>C , CM000681.2:g.46608770T>C	GRCh38
NC_000019.9:g.47112027T>C , CM000681.1:g.47112027T>C	GRCh37
NC_000019.8:g.51803867T>C	NCBI36
NG_051331.1:g.12697T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291295.14:c.286-76T>C MANE Select	ENSP00000291295.8:n.286-76T>C
ENST00000595072.2:n.2715-76T>C
ENST00000602169.2:c.*322-76T>C	ENSP00000499372.1:n.*322-76T>C
ENST00000291295.13:c.286-76T>C	ENSP00000291295.8:n.286-76T>C
ENST00000391918.6:c.178-76T>C	ENSP00000375785.2:n.178-76T>C
ENST00000477244.5:n.410-76T>C
ENST00000482455.5:n.396-76T>C
ENST00000486500.1:n.668T>C
ENST00000594523.5:c.178-76T>C	ENSP00000468877.1:n.178-76T>C
ENST00000595072.1:n.476-76T>C
ENST00000596362.1:c.286-76T>C	ENSP00000472141.1:n.286-76T>C
ENST00000597743.5:c.166-154T>C	ENSP00000470308.1:n.166-154T>C
ENST00000597868.5:n.535T>C
ENST00000598871.5:c.178-76T>C	ENSP00000470502.1:n.178-76T>C
ENST00000599839.5:c.178-76T>C	ENSP00000471225.1:n.178-76T>C
NM_005184.2:c.286-76T>C	NP_005175.2:n.286-76T>C
NM_001329921.1:c.178-76T>C	NP_001316850.1:n.178-76T>C
NM_001329922.1:c.286-76T>C	NP_001316851.1:n.286-76T>C
NM_001329923.1:c.178-76T>C	NP_001316852.1:n.178-76T>C
NM_001329924.1:c.178-76T>C	NP_001316853.1:n.178-76T>C
NM_001329925.1:c.178-76T>C	NP_001316854.1:n.178-76T>C
NM_001329926.1:c.178-76T>C	NP_001316855.1:n.178-76T>C
NM_005184.3:c.286-76T>C	NP_005175.2:n.286-76T>C
NM_001329924.2:c.178-76T>C	NP_001316853.1:n.178-76T>C
NM_001329925.2:c.178-76T>C	NP_001316854.1:n.178-76T>C
NM_001329926.2:c.178-76T>C	NP_001316855.1:n.178-76T>C
NM_005184.4:c.286-76T>C MANE Select	NP_005175.2:n.286-76T>C