Canonical Allele Identifier: CA2579771121

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404433_90404435delinsCCT , CM000676.2:g.90404433_90404435delinsCCT	GRCh38
NC_000014.8:g.90870777_90870779delinsCCT , CM000676.1:g.90870777_90870779delinsCCT	GRCh37
NC_000014.7:g.89940530_89940532delinsCCT	NCBI36
NG_013338.1:g.12451_12453delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.340_342delinsCCT MANE Select	ENSP00000349467.4:p.Gly114Pro
ENST00000447653.8:c.232_234delinsCCT	ENSP00000403491.4:p.Gly78Pro
ENST00000659177.1:c.232_234delinsCCT	ENSP00000499421.1:p.Gly78Pro
ENST00000663135.1:c.232_234delinsCCT	ENSP00000499498.1:p.Gly78Pro
ENST00000356978.8:c.340_342delinsCCT	ENSP00000349467.4:p.Gly114Pro
ENST00000447653.7:c.343_345delinsCCT	ENSP00000403491.3:p.Gly115Pro
ENST00000544280.6:c.232_234delinsCCT	ENSP00000442853.2:p.Gly78Pro
ENST00000553422.1:c.212_214delinsCCT	ENSP00000450425.1:p.Arg71ThrfsTer2
ENST00000553542.5:c.232_234delinsCCT	ENSP00000450829.1:p.Gly78Pro
ENST00000553630.1:c.233_235delinsCCT	ENSP00000451646.1:p.Arg78ThrfsTer2
ENST00000553964.5:n.2470_2472delinsCCT
ENST00000554296.1:n.392_394delinsCCT
ENST00000556721.1:n.266_268delinsCCT
ENST00000557020.5:c.232_234delinsCCT	ENSP00000451062.1:p.Gly78Pro
ENST00000626705.2:c.166-24_166-22delinsCCT	ENSP00000486402.1:n.166-24_166-22delinsCCT
NM_006888.4:c.340_342delinsCCT	NP_008819.1:p.Gly114Pro
XM_006720258.2:c.343_345delinsCCT	XP_006720321.1:p.Gly115Pro
NM_001363669.1:c.232_234delinsCCT	NP_001350598.1:p.Gly78Pro
NM_001363670.1:c.343_345delinsCCT	NP_001350599.1:p.Gly115Pro
NM_006888.5:c.340_342delinsCCT	NP_008819.1:p.Gly114Pro
NM_006888.6:c.340_342delinsCCT MANE Select	NP_008819.1:p.Gly114Pro
NM_001363669.2:c.232_234delinsCCT	NP_001350598.1:p.Gly78Pro
NM_001363670.2:c.343_345delinsCCT	NP_001350599.1:p.Gly115Pro