Canonical Allele Identifier: CA2579771300
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404385_90404387delinsCCG , CM000676.2:g.90404385_90404387delinsCCG GRCh38
NC_000014.8:g.90870729_90870731delinsCCG , CM000676.1:g.90870729_90870731delinsCCG GRCh37
NC_000014.7:g.89940482_89940484delinsCCG NCBI36
NG_013338.1:g.12403_12405delinsCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.292_294delinsCCG MANE Select ENSP00000349467.4:p.Asn98Pro
ENST00000447653.8:c.184_186delinsCCG ENSP00000403491.4:p.Asn62Pro
ENST00000659177.1:c.184_186delinsCCG ENSP00000499421.1:p.Asn62Pro
ENST00000663135.1:c.184_186delinsCCG ENSP00000499498.1:p.Asn62Pro
ENST00000356978.8:c.292_294delinsCCG ENSP00000349467.4:p.Asn98Pro
ENST00000447653.7:c.295_297delinsCCG ENSP00000403491.3:p.Asn99Pro
ENST00000544280.6:c.184_186delinsCCG ENSP00000442853.2:p.Asn62Pro
ENST00000553422.1:c.178-14_178-12delinsCCG ENSP00000450425.1:n.178-14_178-12delinsCCG
ENST00000553542.5:c.184_186delinsCCG ENSP00000450829.1:p.Asn62Pro
ENST00000553630.1:c.185_187delinsCCG ENSP00000451646.1:p.Gln62_Trp63delinsProGly
ENST00000553964.5:n.2422_2424delinsCCG
ENST00000554296.1:n.344_346delinsCCG
ENST00000556721.1:n.218_220delinsCCG
ENST00000557020.5:c.184_186delinsCCG ENSP00000451062.1:p.Asn62Pro
ENST00000626705.2:c.166-72_166-70delinsCCG ENSP00000486402.1:n.166-72_166-70delinsCCG
NM_006888.4:c.292_294delinsCCG NP_008819.1:p.Asn98Pro
XM_006720258.2:c.295_297delinsCCG XP_006720321.1:p.Asn99Pro
NM_001363669.1:c.184_186delinsCCG NP_001350598.1:p.Asn62Pro
NM_001363670.1:c.295_297delinsCCG NP_001350599.1:p.Asn99Pro
NM_006888.5:c.292_294delinsCCG NP_008819.1:p.Asn98Pro
NM_006888.6:c.292_294delinsCCG MANE Select NP_008819.1:p.Asn98Pro
NM_001363669.2:c.184_186delinsCCG NP_001350598.1:p.Asn62Pro
NM_001363670.2:c.295_297delinsCCG NP_001350599.1:p.Asn99Pro