Canonical Allele Identifier: CA2579772492

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404394_90404395delinsGC , CM000676.2:g.90404394_90404395delinsGC	GRCh38
NC_000014.8:g.90870738_90870739delinsGC , CM000676.1:g.90870738_90870739delinsGC	GRCh37
NC_000014.7:g.89940491_89940492delinsGC	NCBI36
NG_013338.1:g.12412_12413delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.301_302delinsGC MANE Select	ENSP00000349467.4:p.Ile101Ala
ENST00000447653.8:c.193_194delinsGC	ENSP00000403491.4:p.Ile65Ala
ENST00000659177.1:c.193_194delinsGC	ENSP00000499421.1:p.Ile65Ala
ENST00000663135.1:c.193_194delinsGC	ENSP00000499498.1:p.Ile65Ala
ENST00000356978.8:c.301_302delinsGC	ENSP00000349467.4:p.Ile101Ala
ENST00000447653.7:c.304_305delinsGC	ENSP00000403491.3:p.Ile102Ala
ENST00000544280.6:c.193_194delinsGC	ENSP00000442853.2:p.Ile65Ala
ENST00000553422.1:c.178-5_178-4delinsGC	ENSP00000450425.1:n.178-5_178-4delinsGC
ENST00000553542.5:c.193_194delinsGC	ENSP00000450829.1:p.Ile65Ala
ENST00000553630.1:c.194_195delinsGC	ENSP00000451646.1:p.Tyr65Cys
ENST00000553964.5:n.2431_2432delinsGC
ENST00000554296.1:n.353_354delinsGC
ENST00000556721.1:n.227_228delinsGC
ENST00000557020.5:c.193_194delinsGC	ENSP00000451062.1:p.Ile65Ala
ENST00000626705.2:c.166-63_166-62delinsGC	ENSP00000486402.1:n.166-63_166-62delinsGC
NM_006888.4:c.301_302delinsGC	NP_008819.1:p.Ile101Ala
XM_006720258.2:c.304_305delinsGC	XP_006720321.1:p.Ile102Ala
NM_001363669.1:c.193_194delinsGC	NP_001350598.1:p.Ile65Ala
NM_001363670.1:c.304_305delinsGC	NP_001350599.1:p.Ile102Ala
NM_006888.5:c.301_302delinsGC	NP_008819.1:p.Ile101Ala
NM_006888.6:c.301_302delinsGC MANE Select	NP_008819.1:p.Ile101Ala
NM_001363669.2:c.193_194delinsGC	NP_001350598.1:p.Ile65Ala
NM_001363670.2:c.304_305delinsGC	NP_001350599.1:p.Ile102Ala