Canonical Allele Identifier: CA2579772349

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404391_90404393delinsACC , CM000676.2:g.90404391_90404393delinsACC	GRCh38
NC_000014.8:g.90870735_90870737delinsACC , CM000676.1:g.90870735_90870737delinsACC	GRCh37
NC_000014.7:g.89940488_89940490delinsACC	NCBI36
NG_013338.1:g.12409_12411delinsACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.298_300delinsACC MANE Select	ENSP00000349467.4:p.Tyr100Thr
ENST00000447653.8:c.190_192delinsACC	ENSP00000403491.4:p.Tyr64Thr
ENST00000659177.1:c.190_192delinsACC	ENSP00000499421.1:p.Tyr64Thr
ENST00000663135.1:c.190_192delinsACC	ENSP00000499498.1:p.Tyr64Thr
ENST00000356978.8:c.298_300delinsACC	ENSP00000349467.4:p.Tyr100Thr
ENST00000447653.7:c.301_303delinsACC	ENSP00000403491.3:p.Tyr101Thr
ENST00000544280.6:c.190_192delinsACC	ENSP00000442853.2:p.Tyr64Thr
ENST00000553422.1:c.178-8_178-6delinsACC	ENSP00000450425.1:n.178-8_178-6delinsACC
ENST00000553542.5:c.190_192delinsACC	ENSP00000450829.1:p.Tyr64Thr
ENST00000553630.1:c.191_193delinsACC	ENSP00000451646.1:p.Leu64_Tyr65delinsTyrHis
ENST00000553964.5:n.2428_2430delinsACC
ENST00000554296.1:n.350_352delinsACC
ENST00000556721.1:n.224_226delinsACC
ENST00000557020.5:c.190_192delinsACC	ENSP00000451062.1:p.Tyr64Thr
ENST00000626705.2:c.166-66_166-64delinsACC	ENSP00000486402.1:n.166-66_166-64delinsACC
NM_006888.4:c.298_300delinsACC	NP_008819.1:p.Tyr100Thr
XM_006720258.2:c.301_303delinsACC	XP_006720321.1:p.Tyr101Thr
NM_001363669.1:c.190_192delinsACC	NP_001350598.1:p.Tyr64Thr
NM_001363670.1:c.301_303delinsACC	NP_001350599.1:p.Tyr101Thr
NM_006888.5:c.298_300delinsACC	NP_008819.1:p.Tyr100Thr
NM_006888.6:c.298_300delinsACC MANE Select	NP_008819.1:p.Tyr100Thr
NM_001363669.2:c.190_192delinsACC	NP_001350598.1:p.Tyr64Thr
NM_001363670.2:c.301_303delinsACC	NP_001350599.1:p.Tyr101Thr