Canonical Allele Identifier: CA2579770466
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404433_90404434delinsCT , CM000676.2:g.90404433_90404434delinsCT GRCh38
NC_000014.8:g.90870777_90870778delinsCT , CM000676.1:g.90870777_90870778delinsCT GRCh37
NC_000014.7:g.89940530_89940531delinsCT NCBI36
NG_013338.1:g.12451_12452delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.340_341delinsCT MANE Select ENSP00000349467.4:p.Gly114Leu
ENST00000447653.8:c.232_233delinsCT ENSP00000403491.4:p.Gly78Leu
ENST00000659177.1:c.232_233delinsCT ENSP00000499421.1:p.Gly78Leu
ENST00000663135.1:c.232_233delinsCT ENSP00000499498.1:p.Gly78Leu
ENST00000356978.8:c.340_341delinsCT ENSP00000349467.4:p.Gly114Leu
ENST00000447653.7:c.343_344delinsCT ENSP00000403491.3:p.Gly115Leu
ENST00000544280.6:c.232_233delinsCT ENSP00000442853.2:p.Gly78Leu
ENST00000553422.1:c.212_213delinsCT ENSP00000450425.1:p.Arg71Thr
ENST00000553542.5:c.232_233delinsCT ENSP00000450829.1:p.Gly78Leu
ENST00000553630.1:c.233_234delinsCT ENSP00000451646.1:p.Arg78Thr
ENST00000553964.5:n.2470_2471delinsCT
ENST00000554296.1:n.392_393delinsCT
ENST00000556721.1:n.266_267delinsCT
ENST00000557020.5:c.232_233delinsCT ENSP00000451062.1:p.Gly78Leu
ENST00000626705.2:c.166-24_166-23delinsCT ENSP00000486402.1:n.166-24_166-23delinsCT
NM_006888.4:c.340_341delinsCT NP_008819.1:p.Gly114Leu
XM_006720258.2:c.343_344delinsCT XP_006720321.1:p.Gly115Leu
NM_001363669.1:c.232_233delinsCT NP_001350598.1:p.Gly78Leu
NM_001363670.1:c.343_344delinsCT NP_001350599.1:p.Gly115Leu
NM_006888.5:c.340_341delinsCT NP_008819.1:p.Gly114Leu
NM_006888.6:c.340_341delinsCT MANE Select NP_008819.1:p.Gly114Leu
NM_001363669.2:c.232_233delinsCT NP_001350598.1:p.Gly78Leu
NM_001363670.2:c.343_344delinsCT NP_001350599.1:p.Gly115Leu