Canonical Allele Identifier: CA2579771889
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404401_90404402delinsAT , CM000676.2:g.90404401_90404402delinsAT GRCh38
NC_000014.8:g.90870745_90870746delinsAT , CM000676.1:g.90870745_90870746delinsAT GRCh37
NC_000014.7:g.89940498_89940499delinsAT NCBI36
NG_013338.1:g.12419_12420delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.308_309delinsAT MANE Select ENSP00000349467.4:p.Ala103Asp
ENST00000447653.8:c.200_201delinsAT ENSP00000403491.4:p.Ala67Asp
ENST00000659177.1:c.200_201delinsAT ENSP00000499421.1:p.Ala67Asp
ENST00000663135.1:c.200_201delinsAT ENSP00000499498.1:p.Ala67Asp
ENST00000356978.8:c.308_309delinsAT ENSP00000349467.4:p.Ala103Asp
ENST00000447653.7:c.311_312delinsAT ENSP00000403491.3:p.Ala104Asp
ENST00000544280.6:c.200_201delinsAT ENSP00000442853.2:p.Ala67Asp
ENST00000553422.1:c.180_181delinsAT ENSP00000450425.1:p.Cys60Ter
ENST00000553542.5:c.200_201delinsAT ENSP00000450829.1:p.Ala67Asp
ENST00000553630.1:c.201_202delinsAT ENSP00000451646.1:p.Cys67Ter
ENST00000553964.5:n.2438_2439delinsAT
ENST00000554296.1:n.360_361delinsAT
ENST00000556721.1:n.234_235delinsAT
ENST00000557020.5:c.200_201delinsAT ENSP00000451062.1:p.Ala67Asp
ENST00000626705.2:c.166-56_166-55delinsAT ENSP00000486402.1:n.166-56_166-55delinsAT
NM_006888.4:c.308_309delinsAT NP_008819.1:p.Ala103Asp
XM_006720258.2:c.311_312delinsAT XP_006720321.1:p.Ala104Asp
NM_001363669.1:c.200_201delinsAT NP_001350598.1:p.Ala67Asp
NM_001363670.1:c.311_312delinsAT NP_001350599.1:p.Ala104Asp
NM_006888.5:c.308_309delinsAT NP_008819.1:p.Ala103Asp
NM_006888.6:c.308_309delinsAT MANE Select NP_008819.1:p.Ala103Asp
NM_001363669.2:c.200_201delinsAT NP_001350598.1:p.Ala67Asp
NM_001363670.2:c.311_312delinsAT NP_001350599.1:p.Ala104Asp