Canonical Allele Identifier: CA2579772383

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404395_90404396delinsCT , CM000676.2:g.90404395_90404396delinsCT	GRCh38
NC_000014.8:g.90870739_90870740delinsCT , CM000676.1:g.90870739_90870740delinsCT	GRCh37
NC_000014.7:g.89940492_89940493delinsCT	NCBI36
NG_013338.1:g.12413_12414delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.302_303delinsCT MANE Select	ENSP00000349467.4:p.Ile101Thr
ENST00000447653.8:c.194_195delinsCT	ENSP00000403491.4:p.Ile65Thr
ENST00000659177.1:c.194_195delinsCT	ENSP00000499421.1:p.Ile65Thr
ENST00000663135.1:c.194_195delinsCT	ENSP00000499498.1:p.Ile65Thr
ENST00000356978.8:c.302_303delinsCT	ENSP00000349467.4:p.Ile101Thr
ENST00000447653.7:c.305_306delinsCT	ENSP00000403491.3:p.Ile102Thr
ENST00000544280.6:c.194_195delinsCT	ENSP00000442853.2:p.Ile65Thr
ENST00000553422.1:c.178-4_178-3delinsCT	ENSP00000450425.1:n.178-4_178-3delinsCT
ENST00000553542.5:c.194_195delinsCT	ENSP00000450829.1:p.Ile65Thr
ENST00000553630.1:c.195_196delinsCT	ENSP00000451646.1:p.Tyr66Ter
ENST00000553964.5:n.2432_2433delinsCT
ENST00000554296.1:n.354_355delinsCT
ENST00000556721.1:n.228_229delinsCT
ENST00000557020.5:c.194_195delinsCT	ENSP00000451062.1:p.Ile65Thr
ENST00000626705.2:c.166-62_166-61delinsCT	ENSP00000486402.1:n.166-62_166-61delinsCT
NM_006888.4:c.302_303delinsCT	NP_008819.1:p.Ile101Thr
XM_006720258.2:c.305_306delinsCT	XP_006720321.1:p.Ile102Thr
NM_001363669.1:c.194_195delinsCT	NP_001350598.1:p.Ile65Thr
NM_001363670.1:c.305_306delinsCT	NP_001350599.1:p.Ile102Thr
NM_006888.5:c.302_303delinsCT	NP_008819.1:p.Ile101Thr
NM_006888.6:c.302_303delinsCT MANE Select	NP_008819.1:p.Ile101Thr
NM_001363669.2:c.194_195delinsCT	NP_001350598.1:p.Ile65Thr
NM_001363670.2:c.305_306delinsCT	NP_001350599.1:p.Ile102Thr