Canonical Allele Identifier: CA2154483906
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404307G= , CM000676.2:g.90404307G= GRCh38
NC_000014.8:g.90870651G= , CM000676.1:g.90870651G= GRCh37
NC_000014.7:g.89940404G= NCBI36
NG_013338.1:g.12325G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.286-72G= MANE Select ENSP00000349467.4:n.286-72G=
ENST00000447653.8:c.178-72G= ENSP00000403491.4:n.178-72G=
ENST00000659177.1:c.178-72G= ENSP00000499421.1:n.178-72G=
ENST00000663135.1:c.178-72G= ENSP00000499498.1:n.178-72G=
ENST00000356978.8:c.286-72G= ENSP00000349467.4:n.286-72G=
ENST00000447653.7:c.289-72G= ENSP00000403491.3:n.289-72G=
ENST00000544280.6:c.178-72G= ENSP00000442853.2:n.178-72G=
ENST00000553422.1:c.178-92G= ENSP00000450425.1:n.178-92G=
ENST00000553542.5:c.178-72G= ENSP00000450829.1:n.178-72G=
ENST00000553630.1:c.179-72G= ENSP00000451646.1:n.179-72G=
ENST00000553964.5:n.2416-72G=
ENST00000554296.1:n.338-72G=
ENST00000556721.1:n.140G=
ENST00000557020.5:c.178-72G= ENSP00000451062.1:n.178-72G=
ENST00000626705.2:c.166-150G= ENSP00000486402.1:n.166-150G=
NM_006888.4:c.286-72G= NP_008819.1:n.286-72G=
XM_006720258.2:c.289-72G= XP_006720321.1:n.289-72G=
NM_001363669.1:c.178-72G= NP_001350598.1:n.178-72G=
NM_001363670.1:c.289-72G= NP_001350599.1:n.289-72G=
NM_006888.5:c.286-72G= NP_008819.1:n.286-72G=
NM_006888.6:c.286-72G= MANE Select NP_008819.1:n.286-72G=
NM_001363669.2:c.178-72G= NP_001350598.1:n.178-72G=
NM_001363670.2:c.289-72G= NP_001350599.1:n.289-72G=