Canonical Allele Identifier: CA2579773441
Gene: CALM1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.90404389_90404390delinsAG , CM000676.2:g.90404389_90404390delinsAG GRCh38
NC_000014.8:g.90870733_90870734delinsAG , CM000676.1:g.90870733_90870734delinsAG GRCh37
NC_000014.7:g.89940486_89940487delinsAG NCBI36
NG_013338.1:g.12407_12408delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000356978.9:c.296_297delinsAG MANE Select ENSP00000349467.4:p.Gly99Glu
ENST00000447653.8:c.188_189delinsAG ENSP00000403491.4:p.Gly63Glu
ENST00000659177.1:c.188_189delinsAG ENSP00000499421.1:p.Gly63Glu
ENST00000663135.1:c.188_189delinsAG ENSP00000499498.1:p.Gly63Glu
ENST00000356978.8:c.296_297delinsAG ENSP00000349467.4:p.Gly99Glu
ENST00000447653.7:c.299_300delinsAG ENSP00000403491.3:p.Gly100Glu
ENST00000544280.6:c.188_189delinsAG ENSP00000442853.2:p.Gly63Glu
ENST00000553422.1:c.178-10_178-9delinsAG ENSP00000450425.1:n.178-10_178-9delinsAG
ENST00000553542.5:c.188_189delinsAG ENSP00000450829.1:p.Gly63Glu
ENST00000553630.1:c.189_190delinsAG ENSP00000451646.1:p.Trp63Ter
ENST00000553964.5:n.2426_2427delinsAG
ENST00000554296.1:n.348_349delinsAG
ENST00000556721.1:n.222_223delinsAG
ENST00000557020.5:c.188_189delinsAG ENSP00000451062.1:p.Gly63Glu
ENST00000626705.2:c.166-68_166-67delinsAG ENSP00000486402.1:n.166-68_166-67delinsAG
NM_006888.4:c.296_297delinsAG NP_008819.1:p.Gly99Glu
XM_006720258.2:c.299_300delinsAG XP_006720321.1:p.Gly100Glu
NM_001363669.1:c.188_189delinsAG NP_001350598.1:p.Gly63Glu
NM_001363670.1:c.299_300delinsAG NP_001350599.1:p.Gly100Glu
NM_006888.5:c.296_297delinsAG NP_008819.1:p.Gly99Glu
NM_006888.6:c.296_297delinsAG MANE Select NP_008819.1:p.Gly99Glu
NM_001363669.2:c.188_189delinsAG NP_001350598.1:p.Gly63Glu
NM_001363670.2:c.299_300delinsAG NP_001350599.1:p.Gly100Glu