Canonical Allele Identifier: CA2572942517
Gene: CALM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404320T>G , CM000676.2:g.90404320T>G GRCh38
NC_000014.8:g.90870664T>G , CM000676.1:g.90870664T>G GRCh37
NC_000014.7:g.89940417T>G NCBI36
NG_013338.1:g.12338T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.286-59T>G MANE Select ENSP00000349467.4:n.286-59T>G
ENST00000447653.8:c.178-59T>G ENSP00000403491.4:n.178-59T>G
ENST00000659177.1:c.178-59T>G ENSP00000499421.1:n.178-59T>G
ENST00000663135.1:c.178-59T>G ENSP00000499498.1:n.178-59T>G
ENST00000356978.8:c.286-59T>G ENSP00000349467.4:n.286-59T>G
ENST00000447653.7:c.289-59T>G ENSP00000403491.3:n.289-59T>G
ENST00000544280.6:c.178-59T>G ENSP00000442853.2:n.178-59T>G
ENST00000553422.1:c.178-79T>G ENSP00000450425.1:n.178-79T>G
ENST00000553542.5:c.178-59T>G ENSP00000450829.1:n.178-59T>G
ENST00000553630.1:c.179-59T>G ENSP00000451646.1:n.179-59T>G
ENST00000553964.5:n.2416-59T>G
ENST00000554296.1:n.338-59T>G
ENST00000556721.1:n.153T>G
ENST00000557020.5:c.178-59T>G ENSP00000451062.1:n.178-59T>G
ENST00000626705.2:c.166-137T>G ENSP00000486402.1:n.166-137T>G
NM_006888.4:c.286-59T>G NP_008819.1:n.286-59T>G
XM_006720258.2:c.289-59T>G XP_006720321.1:n.289-59T>G
NM_001363669.1:c.178-59T>G NP_001350598.1:n.178-59T>G
NM_001363670.1:c.289-59T>G NP_001350599.1:n.289-59T>G
NM_006888.5:c.286-59T>G NP_008819.1:n.286-59T>G
NM_006888.6:c.286-59T>G MANE Select NP_008819.1:n.286-59T>G
NM_001363669.2:c.178-59T>G NP_001350598.1:n.178-59T>G
NM_001363670.2:c.289-59T>G NP_001350599.1:n.289-59T>G