Canonical Allele Identifier: CA390690222
Gene: CALM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404433G>C , CM000676.2:g.90404433G>C GRCh38
NC_000014.8:g.90870777G>C , CM000676.1:g.90870777G>C GRCh37
NC_000014.7:g.89940530G>C NCBI36
NG_013338.1:g.12451G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.340G>C MANE Select ENSP00000349467.4:p.Gly114Arg
ENST00000447653.8:c.232G>C ENSP00000403491.4:p.Gly78Arg
ENST00000659177.1:c.232G>C ENSP00000499421.1:p.Gly78Arg
ENST00000663135.1:c.232G>C ENSP00000499498.1:p.Gly78Arg
ENST00000356978.8:c.340G>C ENSP00000349467.4:p.Gly114Arg
ENST00000447653.7:c.343G>C ENSP00000403491.3:p.Gly115Arg
ENST00000544280.6:c.232G>C ENSP00000442853.2:p.Gly78Arg
ENST00000553422.1:c.212G>C ENSP00000450425.1:p.Arg71Thr
ENST00000553542.5:c.232G>C ENSP00000450829.1:p.Gly78Arg
ENST00000553630.1:c.233G>C ENSP00000451646.1:p.Arg78Thr
ENST00000553964.5:n.2470G>C
ENST00000554296.1:n.392G>C
ENST00000556721.1:n.266G>C
ENST00000557020.5:c.232G>C ENSP00000451062.1:p.Gly78Arg
ENST00000626705.2:c.166-24G>C ENSP00000486402.1:n.166-24G>C
NM_006888.4:c.340G>C NP_008819.1:p.Gly114Arg
XM_006720258.2:c.343G>C XP_006720321.1:p.Gly115Arg
NM_001363669.1:c.232G>C NP_001350598.1:p.Gly78Arg
NM_001363670.1:c.343G>C NP_001350599.1:p.Gly115Arg
NM_006888.5:c.340G>C NP_008819.1:p.Gly114Arg
NM_006888.6:c.340G>C MANE Select NP_008819.1:p.Gly114Arg
NM_001363669.2:c.232G>C NP_001350598.1:p.Gly78Arg
NM_001363670.2:c.343G>C NP_001350599.1:p.Gly115Arg