Canonical Allele Identifier: CA2338996116

Gene: CALM3

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.46608569C= , CM000681.2:g.46608569C=	GRCh38
NC_000019.9:g.47111826C= , CM000681.1:g.47111826C=	GRCh37
NC_000019.8:g.51803666C=	NCBI36
NG_051331.1:g.12496C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000291295.14:c.266C= MANE Select	ENSP00000291295.8:p.Ala89=
ENST00000595072.2:n.2695C=
ENST00000602169.2:c.*302C=	ENSP00000499372.1:n.*302C=
ENST00000291295.13:c.266C=	ENSP00000291295.8:p.Ala89=
ENST00000391918.6:c.158C=	ENSP00000375785.2:p.Ala53=
ENST00000477244.5:n.390C=
ENST00000482455.5:n.376C=
ENST00000486500.1:n.467C=
ENST00000594523.5:c.158C=	ENSP00000468877.1:p.Ala53=
ENST00000595072.1:n.456C=
ENST00000596362.1:c.266C=	ENSP00000472141.1:p.Ala89=
ENST00000597743.5:c.165+242C=	ENSP00000470308.1:n.165+242C=
ENST00000597868.5:n.334C=
ENST00000598871.5:c.158C=	ENSP00000470502.1:p.Ala53=
ENST00000599839.5:c.158C=	ENSP00000471225.1:p.Ala53=
NM_005184.2:c.266C=	NP_005175.2:p.Ala89=
NM_001329921.1:c.158C=	NP_001316850.1:p.Ala53=
NM_001329922.1:c.266C=	NP_001316851.1:p.Ala89=
NM_001329923.1:c.158C=	NP_001316852.1:p.Ala53=
NM_001329924.1:c.158C=	NP_001316853.1:p.Ala53=
NM_001329925.1:c.158C=	NP_001316854.1:p.Ala53=
NM_001329926.1:c.158C=	NP_001316855.1:p.Ala53=
NM_005184.3:c.266C=	NP_005175.2:p.Ala89=
NM_001329924.2:c.158C=	NP_001316853.1:p.Ala53=
NM_001329925.2:c.158C=	NP_001316854.1:p.Ala53=
NM_001329926.2:c.158C=	NP_001316855.1:p.Ala53=
NM_005184.4:c.266C= MANE Select	NP_005175.2:p.Ala89=