Canonical Allele Identifier: CA2338996282

Gene: CALM3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608968G= , CM000681.2:g.46608968G=	GRCh38
NC_000019.9:g.47112225G= , CM000681.1:g.47112225G=	GRCh37
NC_000019.8:g.51804065G=	NCBI36
NG_051331.1:g.12895G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000291295.14:c.408G= MANE Select	ENSP00000291295.8:p.Gln136=
ENST00000595072.2:n.2837G=
ENST00000602169.2:c.*444G=	ENSP00000499372.1:n.*444G=
ENST00000291295.13:c.408G=	ENSP00000291295.8:p.Gln136=
ENST00000391918.6:c.300G=	ENSP00000375785.2:p.Gln100=
ENST00000477244.5:n.532G=
ENST00000482455.5:n.518G=
ENST00000486500.1:n.866G=
ENST00000594523.5:c.300G=	ENSP00000468877.1:p.Gln100=
ENST00000595072.1:n.598G=
ENST00000596362.1:c.408G=	ENSP00000472141.1:p.Gln136=
ENST00000597743.5:c.210G=	ENSP00000470308.1:p.Gln70=
ENST00000597868.5:n.733G=
ENST00000598871.5:c.300G=	ENSP00000470502.1:p.Gln100=
ENST00000599839.5:c.300G=	ENSP00000471225.1:p.Gln100=
NM_005184.2:c.408G=	NP_005175.2:p.Gln136=
NM_001329921.1:c.300G=	NP_001316850.1:p.Gln100=
NM_001329922.1:c.408G=	NP_001316851.1:p.Gln136=
NM_001329923.1:c.300G=	NP_001316852.1:p.Gln100=
NM_001329924.1:c.300G=	NP_001316853.1:p.Gln100=
NM_001329925.1:c.300G=	NP_001316854.1:p.Gln100=
NM_001329926.1:c.300G=	NP_001316855.1:p.Gln100=
NM_005184.3:c.408G=	NP_005175.2:p.Gln136=
NM_001329924.2:c.300G=	NP_001316853.1:p.Gln100=
NM_001329925.2:c.300G=	NP_001316854.1:p.Gln100=
NM_001329926.2:c.300G=	NP_001316855.1:p.Gln100=
NM_005184.4:c.408G= MANE Select	NP_005175.2:p.Gln136=