Canonical Allele Identifier: CA2338996113

Gene: CALM3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608555G= , CM000681.2:g.46608555G=	GRCh38
NC_000019.9:g.47111812G= , CM000681.1:g.47111812G=	GRCh37
NC_000019.8:g.51803652G=	NCBI36
NG_051331.1:g.12482G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291295.14:c.252G= MANE Select	ENSP00000291295.8:p.Glu84=
ENST00000595072.2:n.2681G=
ENST00000602169.2:c.*288G=	ENSP00000499372.1:n.*288G=
ENST00000291295.13:c.252G=	ENSP00000291295.8:p.Glu84=
ENST00000391918.6:c.144G=	ENSP00000375785.2:p.Glu48=
ENST00000477244.5:n.376G=
ENST00000482455.5:n.362G=
ENST00000486500.1:n.453G=
ENST00000594523.5:c.144G=	ENSP00000468877.1:p.Glu48=
ENST00000595072.1:n.442G=
ENST00000596362.1:c.252G=	ENSP00000472141.1:p.Glu84=
ENST00000597743.5:c.165+228G=	ENSP00000470308.1:n.165+228G=
ENST00000597868.5:n.320G=
ENST00000598871.5:c.144G=	ENSP00000470502.1:p.Glu48=
ENST00000599839.5:c.144G=	ENSP00000471225.1:p.Glu48=
NM_005184.2:c.252G=	NP_005175.2:p.Glu84=
NM_001329921.1:c.144G=	NP_001316850.1:p.Glu48=
NM_001329922.1:c.252G=	NP_001316851.1:p.Glu84=
NM_001329923.1:c.144G=	NP_001316852.1:p.Glu48=
NM_001329924.1:c.144G=	NP_001316853.1:p.Glu48=
NM_001329925.1:c.144G=	NP_001316854.1:p.Glu48=
NM_001329926.1:c.144G=	NP_001316855.1:p.Glu48=
NM_005184.3:c.252G=	NP_005175.2:p.Glu84=
NM_001329924.2:c.144G=	NP_001316853.1:p.Glu48=
NM_001329925.2:c.144G=	NP_001316854.1:p.Glu48=
NM_001329926.2:c.144G=	NP_001316855.1:p.Glu48=
NM_005184.4:c.252G= MANE Select	NP_005175.2:p.Glu84=