Canonical Allele Identifier: CA2154484325
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404613G= , CM000676.2:g.90404613G= GRCh38
NC_000014.8:g.90870957G= , CM000676.1:g.90870957G= GRCh37
NC_000014.7:g.89940710G= NCBI36
NG_013338.1:g.12631G=

Transcript Alleles

HGVS Amino-acid change
ENST00000356978.9:c.422-76G= MANE Select ENSP00000349467.4:n.422-76G=
ENST00000447653.8:c.314-76G= ENSP00000403491.4:n.314-76G=
ENST00000659177.1:c.314-76G= ENSP00000499421.1:n.314-76G=
ENST00000663135.1:c.314-76G= ENSP00000499498.1:n.314-76G=
ENST00000356978.8:c.422-76G= ENSP00000349467.4:n.422-76G=
ENST00000447653.7:c.425-76G= ENSP00000403491.3:n.425-76G=
ENST00000544280.6:c.314-76G= ENSP00000442853.2:n.314-76G=
ENST00000553422.1:c.294-76G= ENSP00000450425.1:n.294-76G=
ENST00000553542.5:c.314-76G= ENSP00000450829.1:n.314-76G=
ENST00000553630.1:c.*63-76G= ENSP00000451646.1:n.*63-76G=
ENST00000553964.5:n.2552-76G=
ENST00000554296.1:n.474-76G=
ENST00000556721.1:n.348-76G=
ENST00000626705.2:c.224-76G= ENSP00000486402.1:n.224-76G=
NM_006888.4:c.422-76G= NP_008819.1:n.422-76G=
XM_006720258.2:c.425-76G= XP_006720321.1:n.425-76G=
NM_001363669.1:c.314-76G= NP_001350598.1:n.314-76G=
NM_001363670.1:c.425-76G= NP_001350599.1:n.425-76G=
NM_006888.5:c.422-76G= NP_008819.1:n.422-76G=
NM_006888.6:c.422-76G= MANE Select NP_008819.1:n.422-76G=
NM_001363669.2:c.314-76G= NP_001350598.1:n.314-76G=
NM_001363670.2:c.425-76G= NP_001350599.1:n.425-76G=