Canonical Allele Identifier: CA2579772892

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404389_90404390delinsTG , CM000676.2:g.90404389_90404390delinsTG	GRCh38
NC_000014.8:g.90870733_90870734delinsTG , CM000676.1:g.90870733_90870734delinsTG	GRCh37
NC_000014.7:g.89940486_89940487delinsTG	NCBI36
NG_013338.1:g.12407_12408delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.296_297delinsTG MANE Select	ENSP00000349467.4:p.Gly99Val
ENST00000447653.8:c.188_189delinsTG	ENSP00000403491.4:p.Gly63Val
ENST00000659177.1:c.188_189delinsTG	ENSP00000499421.1:p.Gly63Val
ENST00000663135.1:c.188_189delinsTG	ENSP00000499498.1:p.Gly63Val
ENST00000356978.8:c.296_297delinsTG	ENSP00000349467.4:p.Gly99Val
ENST00000447653.7:c.299_300delinsTG	ENSP00000403491.3:p.Gly100Val
ENST00000544280.6:c.188_189delinsTG	ENSP00000442853.2:p.Gly63Val
ENST00000553422.1:c.178-10_178-9delinsTG	ENSP00000450425.1:n.178-10_178-9delinsTG
ENST00000553542.5:c.188_189delinsTG	ENSP00000450829.1:p.Gly63Val
ENST00000553630.1:c.189_190delinsTG	ENSP00000451646.1:p.Trp63_Leu64delinsCysVal
ENST00000553964.5:n.2426_2427delinsTG
ENST00000554296.1:n.348_349delinsTG
ENST00000556721.1:n.222_223delinsTG
ENST00000557020.5:c.188_189delinsTG	ENSP00000451062.1:p.Gly63Val
ENST00000626705.2:c.166-68_166-67delinsTG	ENSP00000486402.1:n.166-68_166-67delinsTG
NM_006888.4:c.296_297delinsTG	NP_008819.1:p.Gly99Val
XM_006720258.2:c.299_300delinsTG	XP_006720321.1:p.Gly100Val
NM_001363669.1:c.188_189delinsTG	NP_001350598.1:p.Gly63Val
NM_001363670.1:c.299_300delinsTG	NP_001350599.1:p.Gly100Val
NM_006888.5:c.296_297delinsTG	NP_008819.1:p.Gly99Val
NM_006888.6:c.296_297delinsTG MANE Select	NP_008819.1:p.Gly99Val
NM_001363669.2:c.188_189delinsTG	NP_001350598.1:p.Gly63Val
NM_001363670.2:c.299_300delinsTG	NP_001350599.1:p.Gly100Val