Canonical Allele Identifier: CA2579771190

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404382_90404383delinsCT , CM000676.2:g.90404382_90404383delinsCT	GRCh38
NC_000014.8:g.90870726_90870727delinsCT , CM000676.1:g.90870726_90870727delinsCT	GRCh37
NC_000014.7:g.89940479_89940480delinsCT	NCBI36
NG_013338.1:g.12400_12401delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.289_290delinsCT MANE Select	ENSP00000349467.4:p.Gly97Leu
ENST00000447653.8:c.181_182delinsCT	ENSP00000403491.4:p.Gly61Leu
ENST00000659177.1:c.181_182delinsCT	ENSP00000499421.1:p.Gly61Leu
ENST00000663135.1:c.181_182delinsCT	ENSP00000499498.1:p.Gly61Leu
ENST00000356978.8:c.289_290delinsCT	ENSP00000349467.4:p.Gly97Leu
ENST00000447653.7:c.292_293delinsCT	ENSP00000403491.3:p.Gly98Leu
ENST00000544280.6:c.181_182delinsCT	ENSP00000442853.2:p.Gly61Leu
ENST00000553422.1:c.178-17_178-16delinsCT	ENSP00000450425.1:n.178-17_178-16delinsCT
ENST00000553542.5:c.181_182delinsCT	ENSP00000450829.1:p.Gly61Leu
ENST00000553630.1:c.182_183delinsCT	ENSP00000451646.1:p.Trp61Ser
ENST00000553964.5:n.2419_2420delinsCT
ENST00000554296.1:n.341_342delinsCT
ENST00000556721.1:n.215_216delinsCT
ENST00000557020.5:c.181_182delinsCT	ENSP00000451062.1:p.Gly61Leu
ENST00000626705.2:c.166-75_166-74delinsCT	ENSP00000486402.1:n.166-75_166-74delinsCT
NM_006888.4:c.289_290delinsCT	NP_008819.1:p.Gly97Leu
XM_006720258.2:c.292_293delinsCT	XP_006720321.1:p.Gly98Leu
NM_001363669.1:c.181_182delinsCT	NP_001350598.1:p.Gly61Leu
NM_001363670.1:c.292_293delinsCT	NP_001350599.1:p.Gly98Leu
NM_006888.5:c.289_290delinsCT	NP_008819.1:p.Gly97Leu
NM_006888.6:c.289_290delinsCT MANE Select	NP_008819.1:p.Gly97Leu
NM_001363669.2:c.181_182delinsCT	NP_001350598.1:p.Gly61Leu
NM_001363670.2:c.292_293delinsCT	NP_001350599.1:p.Gly98Leu