Canonical Allele Identifier: CA2579773500

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404388_90404390delinsTCG , CM000676.2:g.90404388_90404390delinsTCG	GRCh38
NC_000014.8:g.90870732_90870734delinsTCG , CM000676.1:g.90870732_90870734delinsTCG	GRCh37
NC_000014.7:g.89940485_89940487delinsTCG	NCBI36
NG_013338.1:g.12406_12408delinsTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.295_297delinsTCG MANE Select	ENSP00000349467.4:p.Gly99Ser
ENST00000447653.8:c.187_189delinsTCG	ENSP00000403491.4:p.Gly63Ser
ENST00000659177.1:c.187_189delinsTCG	ENSP00000499421.1:p.Gly63Ser
ENST00000663135.1:c.187_189delinsTCG	ENSP00000499498.1:p.Gly63Ser
ENST00000356978.8:c.295_297delinsTCG	ENSP00000349467.4:p.Gly99Ser
ENST00000447653.7:c.298_300delinsTCG	ENSP00000403491.3:p.Gly100Ser
ENST00000544280.6:c.187_189delinsTCG	ENSP00000442853.2:p.Gly63Ser
ENST00000553422.1:c.178-11_178-9delinsTCG	ENSP00000450425.1:n.178-11_178-9delinsTCG
ENST00000553542.5:c.187_189delinsTCG	ENSP00000450829.1:p.Gly63Ser
ENST00000553630.1:c.188_190delinsTCG	ENSP00000451646.1:p.Trp63_Leu64delinsPheVal
ENST00000553964.5:n.2425_2427delinsTCG
ENST00000554296.1:n.347_349delinsTCG
ENST00000556721.1:n.221_223delinsTCG
ENST00000557020.5:c.187_189delinsTCG	ENSP00000451062.1:p.Gly63Ser
ENST00000626705.2:c.166-69_166-67delinsTCG	ENSP00000486402.1:n.166-69_166-67delinsTCG
NM_006888.4:c.295_297delinsTCG	NP_008819.1:p.Gly99Ser
XM_006720258.2:c.298_300delinsTCG	XP_006720321.1:p.Gly100Ser
NM_001363669.1:c.187_189delinsTCG	NP_001350598.1:p.Gly63Ser
NM_001363670.1:c.298_300delinsTCG	NP_001350599.1:p.Gly100Ser
NM_006888.5:c.295_297delinsTCG	NP_008819.1:p.Gly99Ser
NM_006888.6:c.295_297delinsTCG MANE Select	NP_008819.1:p.Gly99Ser
NM_001363669.2:c.187_189delinsTCG	NP_001350598.1:p.Gly63Ser
NM_001363670.2:c.298_300delinsTCG	NP_001350599.1:p.Gly100Ser