Canonical Allele Identifier: CA2579771707

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404691_90404693delinsCTT , CM000676.2:g.90404691_90404693delinsCTT	GRCh38
NC_000014.8:g.90871035_90871037delinsCTT , CM000676.1:g.90871035_90871037delinsCTT	GRCh37
NC_000014.7:g.89940788_89940790delinsCTT	NCBI36
NG_013338.1:g.12709_12711delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.424_426delinsCTT MANE Select	ENSP00000349467.4:p.Phe142Leu
ENST00000447653.8:c.316_318delinsCTT	ENSP00000403491.4:p.Phe106Leu
ENST00000659177.1:c.316_318delinsCTT	ENSP00000499421.1:p.Phe106Leu
ENST00000663135.1:c.316_318delinsCTT	ENSP00000499498.1:p.Phe106Leu
ENST00000356978.8:c.424_426delinsCTT	ENSP00000349467.4:p.Phe142Leu
ENST00000447653.7:c.427_429delinsCTT	ENSP00000403491.3:p.Phe143Leu
ENST00000544280.6:c.316_318delinsCTT	ENSP00000442853.2:p.Phe106Leu
ENST00000553422.1:c.296_298delinsCTT	ENSP00000450425.1:n.296_298delinsCTT
ENST00000553542.5:c.316_318delinsCTT	ENSP00000450829.1:p.Phe106Leu
ENST00000553630.1:c.*65_*67delinsCTT	ENSP00000451646.1:n.*65_*67delinsCTT
ENST00000553964.5:n.2554_2556delinsCTT
ENST00000554296.1:n.476_478delinsCTT
ENST00000556721.1:n.350_352delinsCTT
ENST00000626705.2:c.226_228delinsCTT	ENSP00000486402.1:p.Phe76Leu
NM_006888.4:c.424_426delinsCTT	NP_008819.1:p.Phe142Leu
XM_006720258.2:c.427_429delinsCTT	XP_006720321.1:p.Phe143Leu
NM_001363669.1:c.316_318delinsCTT	NP_001350598.1:p.Phe106Leu
NM_001363670.1:c.427_429delinsCTT	NP_001350599.1:p.Phe143Leu
NM_006888.5:c.424_426delinsCTT	NP_008819.1:p.Phe142Leu
NM_006888.6:c.424_426delinsCTT MANE Select	NP_008819.1:p.Phe142Leu
NM_001363669.2:c.316_318delinsCTT	NP_001350598.1:p.Phe106Leu
NM_001363670.2:c.427_429delinsCTT	NP_001350599.1:p.Phe143Leu