Canonical Allele Identifier: CA2579772997

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404490_90404492delinsCTG , CM000676.2:g.90404490_90404492delinsCTG	GRCh38
NC_000014.8:g.90870834_90870836delinsCTG , CM000676.1:g.90870834_90870836delinsCTG	GRCh37
NC_000014.7:g.89940587_89940589delinsCTG	NCBI36
NG_013338.1:g.12508_12510delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.397_399delinsCTG MANE Select	ENSP00000349467.4:p.Gly133Leu
ENST00000447653.8:c.289_291delinsCTG	ENSP00000403491.4:p.Gly97Leu
ENST00000659177.1:c.289_291delinsCTG	ENSP00000499421.1:p.Gly97Leu
ENST00000663135.1:c.289_291delinsCTG	ENSP00000499498.1:p.Gly97Leu
ENST00000356978.8:c.397_399delinsCTG	ENSP00000349467.4:p.Gly133Leu
ENST00000447653.7:c.400_402delinsCTG	ENSP00000403491.3:p.Gly134Leu
ENST00000544280.6:c.289_291delinsCTG	ENSP00000442853.2:p.Gly97Leu
ENST00000553422.1:c.269_271delinsCTG	ENSP00000450425.1:n.269_271delinsCTG
ENST00000553542.5:c.289_291delinsCTG	ENSP00000450829.1:p.Gly97Leu
ENST00000553630.1:c.*38_*40delinsCTG	ENSP00000451646.1:n.*38_*40delinsCTG
ENST00000553964.5:n.2527_2529delinsCTG
ENST00000554296.1:n.449_451delinsCTG
ENST00000556721.1:n.323_325delinsCTG
ENST00000557020.5:c.289_291delinsCTG	ENSP00000451062.1:p.Gly97Leu
ENST00000626705.2:c.199_201delinsCTG	ENSP00000486402.1:p.Gly67Leu
NM_006888.4:c.397_399delinsCTG	NP_008819.1:p.Gly133Leu
XM_006720258.2:c.400_402delinsCTG	XP_006720321.1:p.Gly134Leu
NM_001363669.1:c.289_291delinsCTG	NP_001350598.1:p.Gly97Leu
NM_001363670.1:c.400_402delinsCTG	NP_001350599.1:p.Gly134Leu
NM_006888.5:c.397_399delinsCTG	NP_008819.1:p.Gly133Leu
NM_006888.6:c.397_399delinsCTG MANE Select	NP_008819.1:p.Gly133Leu
NM_001363669.2:c.289_291delinsCTG	NP_001350598.1:p.Gly97Leu
NM_001363670.2:c.400_402delinsCTG	NP_001350599.1:p.Gly134Leu