Canonical Allele Identifier: CA2579772572

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404406_90404408delinsTAT , CM000676.2:g.90404406_90404408delinsTAT	GRCh38
NC_000014.8:g.90870750_90870752delinsTAT , CM000676.1:g.90870750_90870752delinsTAT	GRCh37
NC_000014.7:g.89940503_89940505delinsTAT	NCBI36
NG_013338.1:g.12424_12426delinsTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.313_315delinsTAT MANE Select	ENSP00000349467.4:p.Glu105Tyr
ENST00000447653.8:c.205_207delinsTAT	ENSP00000403491.4:p.Glu69Tyr
ENST00000659177.1:c.205_207delinsTAT	ENSP00000499421.1:p.Glu69Tyr
ENST00000663135.1:c.205_207delinsTAT	ENSP00000499498.1:p.Glu69Tyr
ENST00000356978.8:c.313_315delinsTAT	ENSP00000349467.4:p.Glu105Tyr
ENST00000447653.7:c.316_318delinsTAT	ENSP00000403491.3:p.Glu106Tyr
ENST00000544280.6:c.205_207delinsTAT	ENSP00000442853.2:p.Glu69Tyr
ENST00000553422.1:c.185_187delinsTAT	ENSP00000450425.1:p.Arg62_Thr63delinsIleSer
ENST00000553542.5:c.205_207delinsTAT	ENSP00000450829.1:p.Glu69Tyr
ENST00000553630.1:c.206_208delinsTAT	ENSP00000451646.1:p.Arg69_Thr70delinsIleSer
ENST00000553964.5:n.2443_2445delinsTAT
ENST00000554296.1:n.365_367delinsTAT
ENST00000556721.1:n.239_241delinsTAT
ENST00000557020.5:c.205_207delinsTAT	ENSP00000451062.1:p.Glu69Tyr
ENST00000626705.2:c.166-51_166-49delinsTAT	ENSP00000486402.1:n.166-51_166-49delinsTAT
NM_006888.4:c.313_315delinsTAT	NP_008819.1:p.Glu105Tyr
XM_006720258.2:c.316_318delinsTAT	XP_006720321.1:p.Glu106Tyr
NM_001363669.1:c.205_207delinsTAT	NP_001350598.1:p.Glu69Tyr
NM_001363670.1:c.316_318delinsTAT	NP_001350599.1:p.Glu106Tyr
NM_006888.5:c.313_315delinsTAT	NP_008819.1:p.Glu105Tyr
NM_006888.6:c.313_315delinsTAT MANE Select	NP_008819.1:p.Glu105Tyr
NM_001363669.2:c.205_207delinsTAT	NP_001350598.1:p.Glu69Tyr
NM_001363670.2:c.316_318delinsTAT	NP_001350599.1:p.Glu106Tyr