Canonical Allele Identifier: CA2579771556
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404400_90404401delinsTT , CM000676.2:g.90404400_90404401delinsTT GRCh38
NC_000014.8:g.90870744_90870745delinsTT , CM000676.1:g.90870744_90870745delinsTT GRCh37
NC_000014.7:g.89940497_89940498delinsTT NCBI36
NG_013338.1:g.12418_12419delinsTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.307_308delinsTT MANE Select ENSP00000349467.4:p.Ala103Leu
ENST00000447653.8:c.199_200delinsTT ENSP00000403491.4:p.Ala67Leu
ENST00000659177.1:c.199_200delinsTT ENSP00000499421.1:p.Ala67Leu
ENST00000663135.1:c.199_200delinsTT ENSP00000499498.1:p.Ala67Leu
ENST00000356978.8:c.307_308delinsTT ENSP00000349467.4:p.Ala103Leu
ENST00000447653.7:c.310_311delinsTT ENSP00000403491.3:p.Ala104Leu
ENST00000544280.6:c.199_200delinsTT ENSP00000442853.2:p.Ala67Leu
ENST00000553422.1:c.179_180delinsTT ENSP00000450425.1:p.Cys60Phe
ENST00000553542.5:c.199_200delinsTT ENSP00000450829.1:p.Ala67Leu
ENST00000553630.1:c.200_201delinsTT ENSP00000451646.1:p.Cys67Phe
ENST00000553964.5:n.2437_2438delinsTT
ENST00000554296.1:n.359_360delinsTT
ENST00000556721.1:n.233_234delinsTT
ENST00000557020.5:c.199_200delinsTT ENSP00000451062.1:p.Ala67Leu
ENST00000626705.2:c.166-57_166-56delinsTT ENSP00000486402.1:n.166-57_166-56delinsTT
NM_006888.4:c.307_308delinsTT NP_008819.1:p.Ala103Leu
XM_006720258.2:c.310_311delinsTT XP_006720321.1:p.Ala104Leu
NM_001363669.1:c.199_200delinsTT NP_001350598.1:p.Ala67Leu
NM_001363670.1:c.310_311delinsTT NP_001350599.1:p.Ala104Leu
NM_006888.5:c.307_308delinsTT NP_008819.1:p.Ala103Leu
NM_006888.6:c.307_308delinsTT MANE Select NP_008819.1:p.Ala103Leu
NM_001363669.2:c.199_200delinsTT NP_001350598.1:p.Ala67Leu
NM_001363670.2:c.310_311delinsTT NP_001350599.1:p.Ala104Leu