Canonical Allele Identifier: CA390690106
Gene: CALM1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404382G>A , CM000676.2:g.90404382G>A GRCh38
NC_000014.8:g.90870726G>A , CM000676.1:g.90870726G>A GRCh37
NC_000014.7:g.89940479G>A NCBI36
NG_013338.1:g.12400G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.289G>A MANE Select ENSP00000349467.4:p.Gly97Ser
ENST00000447653.8:c.181G>A ENSP00000403491.4:p.Gly61Ser
ENST00000659177.1:c.181G>A ENSP00000499421.1:p.Gly61Ser
ENST00000663135.1:c.181G>A ENSP00000499498.1:p.Gly61Ser
ENST00000356978.8:c.289G>A ENSP00000349467.4:p.Gly97Ser
ENST00000447653.7:c.292G>A ENSP00000403491.3:p.Gly98Ser
ENST00000544280.6:c.181G>A ENSP00000442853.2:p.Gly61Ser
ENST00000553422.1:c.178-17G>A ENSP00000450425.1:n.178-17G>A
ENST00000553542.5:c.181G>A ENSP00000450829.1:p.Gly61Ser
ENST00000553630.1:c.182G>A ENSP00000451646.1:p.Trp61Ter
ENST00000553964.5:n.2419G>A
ENST00000554296.1:n.341G>A
ENST00000556721.1:n.215G>A
ENST00000557020.5:c.181G>A ENSP00000451062.1:p.Gly61Ser
ENST00000626705.2:c.166-75G>A ENSP00000486402.1:n.166-75G>A
NM_006888.4:c.289G>A NP_008819.1:p.Gly97Ser
XM_006720258.2:c.292G>A XP_006720321.1:p.Gly98Ser
NM_001363669.1:c.181G>A NP_001350598.1:p.Gly61Ser
NM_001363670.1:c.292G>A NP_001350599.1:p.Gly98Ser
NM_006888.5:c.289G>A NP_008819.1:p.Gly97Ser
NM_006888.6:c.289G>A MANE Select NP_008819.1:p.Gly97Ser
NM_001363669.2:c.181G>A NP_001350598.1:p.Gly61Ser
NM_001363670.2:c.292G>A NP_001350599.1:p.Gly98Ser