Canonical Allele Identifier: CA2579770147

Gene: CALM1

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.90404400_90404401delinsAG , CM000676.2:g.90404400_90404401delinsAG	GRCh38
NC_000014.8:g.90870744_90870745delinsAG , CM000676.1:g.90870744_90870745delinsAG	GRCh37
NC_000014.7:g.89940497_89940498delinsAG	NCBI36
NG_013338.1:g.12418_12419delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356978.9:c.307_308delinsAG MANE Select	ENSP00000349467.4:p.Ala103Arg
ENST00000447653.8:c.199_200delinsAG	ENSP00000403491.4:p.Ala67Arg
ENST00000659177.1:c.199_200delinsAG	ENSP00000499421.1:p.Ala67Arg
ENST00000663135.1:c.199_200delinsAG	ENSP00000499498.1:p.Ala67Arg
ENST00000356978.8:c.307_308delinsAG	ENSP00000349467.4:p.Ala103Arg
ENST00000447653.7:c.310_311delinsAG	ENSP00000403491.3:p.Ala104Arg
ENST00000544280.6:c.199_200delinsAG	ENSP00000442853.2:p.Ala67Arg
ENST00000553422.1:c.179_180delinsAG	ENSP00000450425.1:p.Cys60Ter
ENST00000553542.5:c.199_200delinsAG	ENSP00000450829.1:p.Ala67Arg
ENST00000553630.1:c.200_201delinsAG	ENSP00000451646.1:p.Cys67Ter
ENST00000553964.5:n.2437_2438delinsAG
ENST00000554296.1:n.359_360delinsAG
ENST00000556721.1:n.233_234delinsAG
ENST00000557020.5:c.199_200delinsAG	ENSP00000451062.1:p.Ala67Arg
ENST00000626705.2:c.166-57_166-56delinsAG	ENSP00000486402.1:n.166-57_166-56delinsAG
NM_006888.4:c.307_308delinsAG	NP_008819.1:p.Ala103Arg
XM_006720258.2:c.310_311delinsAG	XP_006720321.1:p.Ala104Arg
NM_001363669.1:c.199_200delinsAG	NP_001350598.1:p.Ala67Arg
NM_001363670.1:c.310_311delinsAG	NP_001350599.1:p.Ala104Arg
NM_006888.5:c.307_308delinsAG	NP_008819.1:p.Ala103Arg
NM_006888.6:c.307_308delinsAG MANE Select	NP_008819.1:p.Ala103Arg
NM_001363669.2:c.199_200delinsAG	NP_001350598.1:p.Ala67Arg
NM_001363670.2:c.310_311delinsAG	NP_001350599.1:p.Ala104Arg