Canonical Allele Identifier: CA2579769906

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404379_90404380delinsTG , CM000676.2:g.90404379_90404380delinsTG	GRCh38
NC_000014.8:g.90870723_90870724delinsTG , CM000676.1:g.90870723_90870724delinsTG	GRCh37
NC_000014.7:g.89940476_89940477delinsTG	NCBI36
NG_013338.1:g.12397_12398delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.286_287delinsTG MANE Select	ENSP00000349467.4:p.Asp96Cys
ENST00000447653.8:c.178_179delinsTG	ENSP00000403491.4:p.Asp60Cys
ENST00000659177.1:c.178_179delinsTG	ENSP00000499421.1:p.Asp60Cys
ENST00000663135.1:c.178_179delinsTG	ENSP00000499498.1:p.Asp60Cys
ENST00000356978.8:c.286_287delinsTG	ENSP00000349467.4:p.Asp96Cys
ENST00000447653.7:c.289_290delinsTG	ENSP00000403491.3:p.Asp97Cys
ENST00000544280.6:c.178_179delinsTG	ENSP00000442853.2:p.Asp60Cys
ENST00000553422.1:c.178-20_178-19delinsTG	ENSP00000450425.1:n.178-20_178-19delinsTG
ENST00000553542.5:c.178_179delinsTG	ENSP00000450829.1:p.Asp60Cys
ENST00000553630.1:c.179_180delinsTG	ENSP00000451646.1:p.Gly60Val
ENST00000553964.5:n.2416_2417delinsTG
ENST00000554296.1:n.338_339delinsTG
ENST00000556721.1:n.212_213delinsTG
ENST00000557020.5:c.178_179delinsTG	ENSP00000451062.1:p.Asp60Cys
ENST00000626705.2:c.166-78_166-77delinsTG	ENSP00000486402.1:n.166-78_166-77delinsTG
NM_006888.4:c.286_287delinsTG	NP_008819.1:p.Asp96Cys
XM_006720258.2:c.289_290delinsTG	XP_006720321.1:p.Asp97Cys
NM_001363669.1:c.178_179delinsTG	NP_001350598.1:p.Asp60Cys
NM_001363670.1:c.289_290delinsTG	NP_001350599.1:p.Asp97Cys
NM_006888.5:c.286_287delinsTG	NP_008819.1:p.Asp96Cys
NM_006888.6:c.286_287delinsTG MANE Select	NP_008819.1:p.Asp96Cys
NM_001363669.2:c.178_179delinsTG	NP_001350598.1:p.Asp60Cys
NM_001363670.2:c.289_290delinsTG	NP_001350599.1:p.Asp97Cys