Canonical Allele Identifier: CA2579771412

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404394_90404396delinsGCT , CM000676.2:g.90404394_90404396delinsGCT	GRCh38
NC_000014.8:g.90870738_90870740delinsGCT , CM000676.1:g.90870738_90870740delinsGCT	GRCh37
NC_000014.7:g.89940491_89940493delinsGCT	NCBI36
NG_013338.1:g.12412_12414delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.301_303delinsGCT MANE Select	ENSP00000349467.4:p.Ile101Ala
ENST00000447653.8:c.193_195delinsGCT	ENSP00000403491.4:p.Ile65Ala
ENST00000659177.1:c.193_195delinsGCT	ENSP00000499421.1:p.Ile65Ala
ENST00000663135.1:c.193_195delinsGCT	ENSP00000499498.1:p.Ile65Ala
ENST00000356978.8:c.301_303delinsGCT	ENSP00000349467.4:p.Ile101Ala
ENST00000447653.7:c.304_306delinsGCT	ENSP00000403491.3:p.Ile102Ala
ENST00000544280.6:c.193_195delinsGCT	ENSP00000442853.2:p.Ile65Ala
ENST00000553422.1:c.178-5_178-3delinsGCT	ENSP00000450425.1:n.178-5_178-3delinsGCT
ENST00000553542.5:c.193_195delinsGCT	ENSP00000450829.1:p.Ile65Ala
ENST00000553630.1:c.194_196delinsGCT	ENSP00000451646.1:p.Tyr65CysfsTer2
ENST00000553964.5:n.2431_2433delinsGCT
ENST00000554296.1:n.353_355delinsGCT
ENST00000556721.1:n.227_229delinsGCT
ENST00000557020.5:c.193_195delinsGCT	ENSP00000451062.1:p.Ile65Ala
ENST00000626705.2:c.166-63_166-61delinsGCT	ENSP00000486402.1:n.166-63_166-61delinsGCT
NM_006888.4:c.301_303delinsGCT	NP_008819.1:p.Ile101Ala
XM_006720258.2:c.304_306delinsGCT	XP_006720321.1:p.Ile102Ala
NM_001363669.1:c.193_195delinsGCT	NP_001350598.1:p.Ile65Ala
NM_001363670.1:c.304_306delinsGCT	NP_001350599.1:p.Ile102Ala
NM_006888.5:c.301_303delinsGCT	NP_008819.1:p.Ile101Ala
NM_006888.6:c.301_303delinsGCT MANE Select	NP_008819.1:p.Ile101Ala
NM_001363669.2:c.193_195delinsGCT	NP_001350598.1:p.Ile65Ala
NM_001363670.2:c.304_306delinsGCT	NP_001350599.1:p.Ile102Ala