Canonical Allele Identifier: CA2626079448
Gene: CALM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404327_90404328insG , CM000676.2:g.90404327_90404328insG GRCh38
NC_000014.8:g.90870671_90870672insG , CM000676.1:g.90870671_90870672insG GRCh37
NC_000014.7:g.89940424_89940425insG NCBI36
NG_013338.1:g.12345_12346insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.286-52_286-51insG MANE Select ENSP00000349467.4:n.286-52_286-51insG
ENST00000447653.8:c.178-52_178-51insG ENSP00000403491.4:n.178-52_178-51insG
ENST00000659177.1:c.178-52_178-51insG ENSP00000499421.1:n.178-52_178-51insG
ENST00000663135.1:c.178-52_178-51insG ENSP00000499498.1:n.178-52_178-51insG
ENST00000356978.8:c.286-52_286-51insG ENSP00000349467.4:n.286-52_286-51insG
ENST00000447653.7:c.289-52_289-51insG ENSP00000403491.3:n.289-52_289-51insG
ENST00000544280.6:c.178-52_178-51insG ENSP00000442853.2:n.178-52_178-51insG
ENST00000553422.1:c.178-72_178-71insG ENSP00000450425.1:n.178-72_178-71insG
ENST00000553542.5:c.178-52_178-51insG ENSP00000450829.1:n.178-52_178-51insG
ENST00000553630.1:c.179-52_179-51insG ENSP00000451646.1:n.179-52_179-51insG
ENST00000553964.5:n.2416-52_2416-51insG
ENST00000554296.1:n.338-52_338-51insG
ENST00000556721.1:n.160_161insG
ENST00000557020.5:c.178-52_178-51insG ENSP00000451062.1:n.178-52_178-51insG
ENST00000626705.2:c.166-130_166-129insG ENSP00000486402.1:n.166-130_166-129insG
NM_006888.4:c.286-52_286-51insG NP_008819.1:n.286-52_286-51insG
XM_006720258.2:c.289-52_289-51insG XP_006720321.1:n.289-52_289-51insG
NM_001363669.1:c.178-52_178-51insG NP_001350598.1:n.178-52_178-51insG
NM_001363670.1:c.289-52_289-51insG NP_001350599.1:n.289-52_289-51insG
NM_006888.5:c.286-52_286-51insG NP_008819.1:n.286-52_286-51insG
NM_006888.6:c.286-52_286-51insG MANE Select NP_008819.1:n.286-52_286-51insG
NM_001363669.2:c.178-52_178-51insG NP_001350598.1:n.178-52_178-51insG
NM_001363670.2:c.289-52_289-51insG NP_001350599.1:n.289-52_289-51insG