Canonical Allele Identifier: CA2579771720
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404403_90404405delinsCCT , CM000676.2:g.90404403_90404405delinsCCT GRCh38
NC_000014.8:g.90870747_90870749delinsCCT , CM000676.1:g.90870747_90870749delinsCCT GRCh37
NC_000014.7:g.89940500_89940502delinsCCT NCBI36
NG_013338.1:g.12421_12423delinsCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.310_312delinsCCT MANE Select ENSP00000349467.4:p.Ala104Pro
ENST00000447653.8:c.202_204delinsCCT ENSP00000403491.4:p.Ala68Pro
ENST00000659177.1:c.202_204delinsCCT ENSP00000499421.1:p.Ala68Pro
ENST00000663135.1:c.202_204delinsCCT ENSP00000499498.1:p.Ala68Pro
ENST00000356978.8:c.310_312delinsCCT ENSP00000349467.4:p.Ala104Pro
ENST00000447653.7:c.313_315delinsCCT ENSP00000403491.3:p.Ala105Pro
ENST00000544280.6:c.202_204delinsCCT ENSP00000442853.2:p.Ala68Pro
ENST00000553422.1:c.182_184delinsCCT ENSP00000450425.1:p.Ser61ThrfsTer2
ENST00000553542.5:c.202_204delinsCCT ENSP00000450829.1:p.Ala68Pro
ENST00000553630.1:c.203_205delinsCCT ENSP00000451646.1:p.Ser68ThrfsTer2
ENST00000553964.5:n.2440_2442delinsCCT
ENST00000554296.1:n.362_364delinsCCT
ENST00000556721.1:n.236_238delinsCCT
ENST00000557020.5:c.202_204delinsCCT ENSP00000451062.1:p.Ala68Pro
ENST00000626705.2:c.166-54_166-52delinsCCT ENSP00000486402.1:n.166-54_166-52delinsCCT
NM_006888.4:c.310_312delinsCCT NP_008819.1:p.Ala104Pro
XM_006720258.2:c.313_315delinsCCT XP_006720321.1:p.Ala105Pro
NM_001363669.1:c.202_204delinsCCT NP_001350598.1:p.Ala68Pro
NM_001363670.1:c.313_315delinsCCT NP_001350599.1:p.Ala105Pro
NM_006888.5:c.310_312delinsCCT NP_008819.1:p.Ala104Pro
NM_006888.6:c.310_312delinsCCT MANE Select NP_008819.1:p.Ala104Pro
NM_001363669.2:c.202_204delinsCCT NP_001350598.1:p.Ala68Pro
NM_001363670.2:c.313_315delinsCCT NP_001350599.1:p.Ala105Pro